Surgical Operation With Formation of External StomaNCT01600508
Videoconference in Stoma Out-patient Clinic
A study testing Videoconference stoma care in people with Surgical Operation With Formation of External Stoma, run by University Hospital of North Norway.
Trial summary
Background: Videoconference (VC) is a common clinical tool and has huge potential to alter medical practice and to offer patients the best expertise in treatment and follow-up in spite of long distances, especially in rural areas. Studies upon selected patient groups have shown that VC is safe and cost-effective. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Surgical Operation With Formation of External Stoma
- What is being tested?
- Videoconference stoma care
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 110 participants
- Where
- No sites listed yet
- Study dates
- Sep 2011to Dec 2014
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Stoma patients
Who cannot join
- Not able to travel,
- Accepted written consent
About this study
Official title: . A Randomized Controlled Trial Comparing Videoconference and Outpatient Stoma Care
Background:
Videoconference (VC) is a common clinical tool and has huge potential to alter medical practice and to offer patients the best expertise in treatment and follow-up in spite of long distances, especially in rural areas. Studies upon selected patient groups have shown that VC is safe and cost-effective. However, RCT of VC patients with stoma problems have never been performed.
Read more
Patients with stoma problems are resource demanding patients. The University Hospital North Norway (UNN) has several hundred consultations for this patient group each year, serving the population in North Norway.
Methods: In this randomised controlled trial (RCT), patients are either randomised to a VC consultation or a regular consultation at the outpatient clinic. All patients with a stoma that needs special attention are eligible for inclusion. Patients randomised to the VC group, are set-up to a meeting at the nearest VC studio located to their home community. There will be educated VC- stoma nurses that will participate in the clinical examination at the hospital outpatient clinic and at the rural VC studio.
Endpoints: Primary endpoints are patient satisfaction and quality of life. Secondary endpoints are number of consultations and cost effectiveness.
Sample size calculations showed that 170 patients had to be included in the trial.
The investigators hypothesize that postoperative follow-up of stoma patients by VC will not have any impact on patients' quality of life compared to Hospital outpatient follow-up. Furthermore, the investigators hypothesize that the incremental cost-effectiveness ratio will improve.
Read the detailed description
There has been substantial development in the uses of VC among medical personnel [1]. Therefore, new applications of VC are emerging, such as surgical telementoring, trauma and emergency medicine, postoperative follow-up of patients, education of medical personnel, and multidisciplinary team meetings [2]. VC has a great and unused potential, this is recently described in an "invited commentary" in World Journal of Surgery [3]. Furthermore, during recent years, the cost of VC equipment has become less expensive, and advanced technical skills are not required to use the system.
Patients with stoma problems are a large and resource demanding group. Each year there are performed several hundred consultations at the surgical outpatient clinic at University Hospital of North-Norway for this patient group. These patients are surgically treated at the gastrointestinal, urological and gynaecological department.
The visual component is critical to give patients with stoma problems the best care, VC will therefore be well suited for this patient group [4, 5]. Furthermore, the infrastructure for VC in northern Norway is well developed for VC. In the county of Finnmark, Troms and Nordland there are a VC network, all linked together through the Norwegian Health Network.
The purpose of this study is to obtain insight into quality of life (QoL) among patients followed up in a hospital outpatient setting or by VC, and into the incremental cost-effectiveness ratio from the point of view of health care and of society.
Methods and design Study design This study is a randomized controlled trial where patients either will be randomized to follow up at the surgical outpatient clinic (control group) or by VC (intervention group
Participants Patients (inclusion and exclusion criteria's)
Medical doctors
Stoma nurses
Intervention Patients are randomized to follow-up either by VC (intervention) or at the surgical outpatient clinic. All patients will receive their first postoperative check-up at the hospital. A clinical examination will then be performed and information about the RCT given. If the patient gives informed consent, randomization is performed. Patients randomized to VC follow-up are referred to their GP and the local VC stoma nurse.
Control arm Patients in the control group consist of patients randomized to regular follow-up at the hospital's surgical outpatient clinic. This follow-up is performed by consultants in digestive surgery, or a specially educated stoma nurse. QOL questionnaires The EQ-5D questionnaires for the two-year follow-up period (at 1, 3, 6, 9, 12, 15, 18, 21, 24 month follow-up) are given to the patient at baseline examination. Economic evaluation questionnaire: A questionnaire has been developed to enable calculation of costs related to patient examinations. This questionnaire is incorporated in the QOL questionnaire, and patients are requested to fill out the questionnaire at 1, 3 6, 9, 12, 15, 18, 21 and 24 months after inclusion. The cost elements will include patient- and family-related costs due to outpatient visits, VC visits, laboratory tests, radiographs/ultrasound, examinations due to stoma complications, treatment of stoma complications, traveling, production losses, co-payments and other patient expenses. Control arm Patients in the control group consist of patients randomized to regular follow-up at the hospital's surgical outpatient clinic. Consultants in digestive surgery or stoma nurses perform this follow-up.
Objectives Primary objective We aim to compare quality of life and costs of follow-up among patients followed up by VC or at the surgical outpatient clinic. We hypothesize that patients followed up by VC will experience similar or higher scores on quality of life measures and lower costs during follow-up.
Secondary objective We want to establish a nurse led VC stoma school, prior to the clinical trial. Nurses, specially educated to treat patient with stoma problems, will write the curriculum. Five to ten nurses from logistic important VC communities all over North Norway will be invited to a 10 to 20 hour course in stoma treatment and technical aspects around VC. This will be done prior to the start of the clinical study.
Outcome measures Primary outcome (measured at 1, 3, 6,9,12,15,18,21 and 24 months) Quality of life EQ-5D is a standardized generic instrument for use as a measure of health outcome. Applicable to a wide range of health conditions and treatments, it provides a simple descriptive profile and a single index value for health status.
EQ-5D measures five dimensions of health-related quality of life (HRQOL): mobility, self-care, usual activities, pain/discomfort and anxiety/depression. EQ Visual Analogue Scale: The EQ VAS records the respondent's self-rated health status on a vertically graduated (0-100) visual analogue scale [6]. Economic analysis A cost-effectiveness analysis will be performed alongside the randomized controlled trial. A Markov model will be employed. If the trial reveals no difference in health outcomes or quality of life of the patients, a cost-minimization analysis will be carried out. If we reveal a difference in quality of life between the two groups, we will implement a cost-utility analysis. The economic evaluation will have a health care and societal perspective. Resources used in both treatment arms will be registered prospectively based on reports by the patients and on the hospital patient records. Costs related to consultations at the primary and secondary care level, both at baseline and up to 24 months after randomization, including direct medical costs, indirect costs (production losses), travel costs and patient-/family-related costs will be registered. Quality of life measurements will be collected both at baseline and at several time points during the intervention. A 3% discount rate will be used to discount future costs and benefits.
The cost elements will include costs related to outpatient visits, GP visits, laboratory tests, radiographs and ultrasound, examinations due to suspected stoma complications, treatment of stoma complications, traveling/transportation, and production losses, co-payments and other patient/family expenses. The net costs and outcomes of the two treatment options will be compared and presented as incremental cost-effectiveness ratios.
Sample size Sample size calculations are according to Campbell's [7] and EQ-5D guidelines [8]. Alpha and beta were set at 0.05 and 0.2 respectively and tests were two-sided. We hypothesize that patients followed up by VC will have a minor to moderate increase in the QoL scores. Allowing for a dropout rate of 20%, detecting this difference with confidence we required a total sample size of 170 patients.
Randomization Randomization will be done at the 1-month check-up (baseline) after the patients have given informed consent. The randomization service is web-based and managed by the Norwegian University of Science and Technology.
Patients allocated to VC follow-up may be referred back to surgical clinics at any point in the study. Data gathering Data are being collected for patients in the intervention and the control group in identical ways. QoL and "cost questionnaires" are sent after each follow-up appointment by the patients to the trial center up to 24 months postoperatively. These questionnaires are optically readable, data being consecutively collected in a trial database. SCEs are registered via hospital chart review at 24 months postoperatively. The Norwegian Data Inspectorate has approved the study. All data will be handled with strict confidentiality, and study reports or presentations will maintain the anonymity of patients, surgeons, GPs and hospitals. Data collection will be complete by the end of 2013.
Analysis We will use the intention-to-treat principle when analyzing data. Treatment arms will be compared with respect to potential covariates using continuous and categorical univariable analyses. These will include variables relating to patients (age, sex, comorbidities, cost), treatment (surgical resection, surgical complications), hospital surgical outpatient clinic (cost, patient satisfaction, QoL), VC consultation (cost, patient satisfaction, QoL). The cost elements will include costs related to outpatient visits, VC visits, laboratory tests, radiographs/ultrasound, and examinations due to suspected complications, treatment of complications, traveling/transportation, production losses, co-payments and other patient expenses. The net costs and outcomes of the two treatment/follow-up options will be compared and presented as cost-effectiveness ratios. If the trial reveals no difference in health outcomes or quality of life for the patients, a cost-minimization analysis will be carried out. If we find a difference in quality of life or overall survival rates between the two groups, we will use a cost utility approach. The economic evaluation will have a societal and health care perspective. The method of analysis, including adjusting for covariates will comply with the CONSORT statement [9]. The results will be expressed as odds ratios for binary outcomes, hazard ratios for time- to-event outcomes or mean differences for continuous outcomes with corresponding standard errors, 95% confidence intervals, and associated p-values. P-values will be reported to three decimal places with p-values less than 0.001 reported as p < 0.001. For all tests we will use alpha = 0.05 level of significance.
Ethics The Regional Committee for Medical Research Ethics, North Norway approved this protocol. Patients must provide written consent before entering the trial.
Discussion VC is used as an instrument for follow-up of patients in the postoperative period and for outpatient consultation. From our hospital, we have extensive experience in the use of VC in the follow-up of haemodialysis patients [10] and in dermatology [11, 12]. In addition, a new project has started in the orthopaedic department, where a VC line has been established between the University Hospital and the district medical centre Nordreisa, 155 miles away. In this project, both outpatient patients and postoperative patients are examined by a district orthopaedic nurse under the supervision of an orthopaedic consultant located at the University Hospital. This project has now been organized as a randomised controlled trial, where the primary endpoints are cost-effectiveness and patient satisfaction.
Several articles have reported the use of VC in the follow-up of surgical patients. Wallace et al. aimed to compare joint VC between general practitioners, specialists (surgeons), and patients with standard outpatient referral. This randomised controlled trial showed that allocation of patients to virtual outreach consultations was variably associated with increased offers of follow-up appointments according to site and specialty, but led to significant increases in patients' satisfaction and substantial reductions in tests and investigations. Efficient operation of such services will require appropriate selection of patients, significant service reorganization, and provision of logistical support [13].
A study from Finland investigated the use of VC in the examination of orthopaedic outpatients. VC was found to be feasible and the equipment functioned well technically. The conclusion was that VC between primary and secondary care could be used in the examination of orthopaedic patients whenever no demanding imaging technology was needed [14] Whether VC is cost-effective in the follow-up of surgical patients is debated. The clinical effectiveness and costs of VC in orthopaedics between primary and secondary care were examined in an eight-month prospective comparative study. The general surgery outpatient clinics of two Finnish district hospitals were compared. The direct costs of an outpatient visit were 45% greater per patient than for a VC. A cost-minimization analysis of the alternative interventions showed a net benefit of EU 2,500 in favour of VC [15].
Another Finnish study had similar results. Wider utilization of the VC equipment for other purposes, or the use of less expensive VC equipment, would make services cost saving even at relatively short distances [16].
VC can be used in almost any medical specialty, although the specialties best suited are those with a high visual component. Wound healing and wound management are thus prime candidates for VC follow-up. Development of a suitable telemedical system in this field could have a significant effect on wound care in the community, tertiary referral patterns, and hospital admission rates [5, 17].
- Being tested
- Videoconference stoma care
- Keywords
- stoma care, videoconference, costs, quality of life
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Videoconference stoma careOther
Stoma patients are randomized to videoconference stoma care or surgical outpatients clinic stoma care
| Study group | Role | What they receive |
|---|---|---|
| Traditional stoma care | Active comparator | Being discharged from a hospital with a stoma is a challenge to the patient's quality of life in many aspects. Optimal stoma function and care is essential to keep quality of life best possible. Videoconference can be a useful tool to help patients cope with stoma problems without travelling long distances to a surgical outpatient clinic. Receives: Other: Videoconference stoma care |
| Videoconference Stoma Consultations | Experimental | Videoconference Stoma Consultations Receives: Other: Videoconference stoma care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in quality of life
We aim to compare quality of life measured with EQ-5D questionnaires among patients followed up by VC vs those followed up at the surgical outpatient clinic at 1, 3, 6, 9, 12, 15, 18, 21, 24 months of follow-up. We hypothesize that patients followed up by VC will experience similar or higher scores on quality of life measures during followup.
Measured: up to two years
Secondary outcomes (1)
Cost effectiveness
Economic evaluation questionnaire, incorporated in the QOL questionnaire, is given to the patients and requested to fill out at baseline and at 1, 3 6, 9, 12, 15, 18, 21 and 24 months after inclusion. It has been developed to enable calculation of costs related to patient examinations such as patient- and family-related costs due to outpatient visits, VC visits, laboratory tests, radiographs/ultrasound, examinations due stoma complications, treatment of complications, traveling, production losses, co-payments and other patient expenses.
Measured: up to two years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 May 2012 (estimated)
- Study startSep 2011
- Primary completionDec 2014
- Study completionDec 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (18)Papers the sponsor has linked to this study.
- Other trials for Surgical Operation With Formation of External StomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 110 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital of North Norway
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Rolv-Ole Lindsetmo, MD, PhD, MPH, Principal investigator, Institute of Clinical Medicine, Tromsø University, Norway, Univertsity Hospital of North Norway
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01600508
- Sponsor's protocol ID
- 2009/1432a (REK)
- Status last verified
- Jun 2016
- First submitted
- 3 Apr 2012
- Last updated
- 17 Jun 2016
- Results posted
- No
- Data monitoring committee
- No
Publications
Jarvis-Selinger S, Chan E, Payne R, Plohman K, Ho K. Clinical telehealth across the disciplines: lessons learned. Telemed J E Health. 2008 Sep;14(7):720-5. doi: 10.1089/tmj.2007.0108.
PubMed 18817503Augestad KM, Lindsetmo RO. Overcoming distance: video-conferencing as a clinical and educational tool among surgeons. World J Surg. 2009 Jul;33(7):1356-65. doi: 10.1007/s00268-009-0036-0.
PubMed 19384459Doarn CR. The power of video conferencing in surgical practice and education. World J Surg. 2009 Jul;33(7):1366-7. doi: 10.1007/s00268-009-0042-2. No abstract available.
PubMed 19390758Shannon RJ. Telemedicine in wound healing. Int Wound J. 2005 Sep;2(3):239-40. doi: 10.1111/j.1742-4801.2005.0124b.x. No abstract available.
PubMed 16618327Wilbright WA, Birke JA, Patout CA, Varnado M, Horswell R. The use of telemedicine in the management of diabetes-related foot ulceration: a pilot study. Adv Skin Wound Care. 2004 Jun;17(5 Pt 1):232-8. doi: 10.1097/00129334-200406000-00012.
PubMed 15192491EuroQol Group. EuroQol--a new facility for the measurement of health-related quality of life. Health Policy. 1990 Dec;16(3):199-208. doi: 10.1016/0168-8510(90)90421-9.
PubMed 10109801Campbell MJ, Julious SA, Altman DG. Estimating sample sizes for binary, ordered categorical, and continuous outcomes in two group comparisons. BMJ. 1995 Oct 28;311(7013):1145-8. doi: 10.1136/bmj.311.7013.1145.
PubMed 7580713Roset M, Badia X, Mayo NE. Sample size calculations in studies using the EuroQol 5D. Qual Life Res. 1999 Sep;8(6):539-49. doi: 10.1023/a:1008973731515.
PubMed 10548869Moher D, Schulz KF, Altman DG. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet. 2001 Apr 14;357(9263):1191-4.
PubMed 11323066Rumpsfeld M, Arild E, Norum J, Breivik E. Telemedicine in haemodialysis: a university department and two remote satellites linked together as one common workplace. J Telemed Telecare. 2005;11(5):251-5. doi: 10.1258/1357633054471885.
PubMed 16035968Moseng D. [Teledermatology--experiences from Northern Norway]. Tidsskr Nor Laegeforen. 2000 Jun 20;120(16):1893-5. Norwegian.
PubMed 10925620Nordal EJ, Moseng D, Kvammen B, Lochen ML. A comparative study of teleconsultations versus face-to-face consultations. J Telemed Telecare. 2001;7(5):257-65. doi: 10.1258/1357633011936507.
PubMed 11571079Wallace P, Haines A, Harrison R, Barber J, Thompson S, Jacklin P, Roberts J, Lewis L, Wainwright P; Virtual Outreach Project Group. Joint teleconsultations (virtual outreach) versus standard outpatient appointments for patients referred by their general practitioner for a specialist opinion: a randomised trial. Lancet. 2002 Jun 8;359(9322):1961-8. doi: 10.1016/s0140-6736(02)08828-1.
PubMed 12076550Haukipuro K, Ohinmaa A, Winblad I, Linden T, Vuolio S. The feasibility of telemedicine for orthopaedic outpatient clinics--a randomized controlled trial. J Telemed Telecare. 2000;6(4):193-8. doi: 10.1258/1357633001935347.
PubMed 11027118Harno K, Arajarvi E, Paavola T, Carlson C, Viikinkoski P. Clinical effectiveness and cost analysis of patient referral by videoconferencing in orthopaedics. J Telemed Telecare. 2001;7(4):219-25. doi: 10.1258/1357633011936435.
PubMed 11506757
Study at a glance
From the registry record, last updated by the sponsor on 17 Jun 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- . A Randomized Controlled Trial Comparing Videoconference and Outpatient Stoma Care
- ClinicalTrials.gov ID
- NCT01600508
- Acronym / sponsor ID
- 2009/1432a (REK)
- Keywords
- stoma care, videoconference, costs, quality of life
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 110 participants (actual)
- Lead sponsor
- University Hospital of North NorwayUniversity, hospital or other
- Study start
- Sep 2011
- Primary completion
- Dec 2014 (actual)
- Study completion
- Dec 2014 (actual)
- First posted
- 17 May 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background:
Videoconference (VC) is a common clinical tool and has huge potential to alter medical practice and to offer patients the best expertise in treatment and follow-up in spite of long distances, especially in rural areas. Studies upon selected patient groups have shown that VC is safe and cost-effective. However, RCT of VC patients with stoma problems have never been performed.
Patients with stoma problems are resource demanding patients. The University Hospital North Norway (UNN) has several hundred consultations for this patient group each year, serving the population in North Norway.
Methods: In this randomised controlled trial (RCT), patients are either randomised to a VC consultation or a regular consultation at the outpatient clinic. All patients with a stoma that needs special attention are eligible for inclusion. Patients randomised to the VC group, are set-up to a meeting at the nearest VC studio located to their home community. There will be educated VC- stoma nurses that will participate in the clinical examination at the hospital outpatient clinic and at the rural VC studio.
Endpoints: Primary endpoints are patient satisfaction and quality of life. Secondary endpoints are number of consultations and cost effectiveness.
Sample size calculations showed that 170 patients had to be included in the trial.
The investigators hypothesize that postoperative follow-up of stoma patients by VC will not have any impact on patients' quality of life compared to Hospital outpatient follow-up. Furthermore, the investigators hypothesize that the incremental cost-effectiveness ratio will improve.
Detailed description
There has been substantial development in the uses of VC among medical personnel [1]. Therefore, new applications of VC are emerging, such as surgical telementoring, trauma and emergency medicine, postoperative follow-up of patients, education of medical personnel, and multidisciplinary team meetings [2]. VC has a great and unused potential, this is recently described in an "invited commentary" in World Journal of Surgery [3]. Furthermore, during recent years, the cost of VC equipment has become less expensive, and advanced technical skills are not required to use the system.
Patients with stoma problems are a large and resource demanding group. Each year there are performed several hundred consultations at the surgical outpatient clinic at University Hospital of North-Norway for this patient group. These patients are surgically treated at the gastrointestinal, urological and gynaecological department.
The visual component is critical to give patients with stoma problems the best care, VC will therefore be well suited for this patient group [4, 5]. Furthermore, the infrastructure for VC in northern Norway is well developed for VC. In the county of Finnmark, Troms and Nordland there are a VC network, all linked together through the Norwegian Health Network.
The purpose of this study is to obtain insight into quality of life (QoL) among patients followed up in a hospital outpatient setting or by VC, and into the incremental cost-effectiveness ratio from the point of view of health care and of society.
Methods and design Study design This study is a randomized controlled trial where patients either will be randomized to follow up at the surgical outpatient clinic (control group) or by VC (intervention group
Participants Patients (inclusion and exclusion criteria's)
Medical doctors
Stoma nurses
Intervention Patients are randomized to follow-up either by VC (intervention) or at the surgical outpatient clinic. All patients will receive their first postoperative check-up at the hospital. A clinical examination will then be performed and information about the RCT given. If the patient gives informed consent, randomization is performed. Patients randomized to VC follow-up are referred to their GP and the local VC stoma nurse.
Control arm Patients in the control group consist of patients randomized to regular follow-up at the hospital's surgical outpatient clinic. This follow-up is performed by consultants in digestive surgery, or a specially educated stoma nurse. QOL questionnaires The EQ-5D questionnaires for the two-year follow-up period (at 1, 3, 6, 9, 12, 15, 18, 21, 24 month follow-up) are given to the patient at baseline examination. Economic evaluation questionnaire: A questionnaire has been developed to enable calculation of costs related to patient examinations. This questionnaire is incorporated in the QOL questionnaire, and patients are requested to fill out the questionnaire at 1, 3 6, 9, 12, 15, 18, 21 and 24 months after inclusion. The cost elements will include patient- and family-related costs due to outpatient visits, VC visits, laboratory tests, radiographs/ultrasound, examinations due to stoma complications, treatment of stoma complications, traveling, production losses, co-payments and other patient expenses. Control arm Patients in the control group consist of patients randomized to regular follow-up at the hospital's surgical outpatient clinic. Consultants in digestive surgery or stoma nurses perform this follow-up.
Objectives Primary objective We aim to compare quality of life and costs of follow-up among patients followed up by VC or at the surgical outpatient clinic. We hypothesize that patients followed up by VC will experience similar or higher scores on quality of life measures and lower costs during follow-up.
Secondary objective We want to establish a nurse led VC stoma school, prior to the clinical trial. Nurses, specially educated to treat patient with stoma problems, will write the curriculum. Five to ten nurses from logistic important VC communities all over North Norway will be invited to a 10 to 20 hour course in stoma treatment and technical aspects around VC. This will be done prior to the start of the clinical study.
Outcome measures Primary outcome (measured at 1, 3, 6,9,12,15,18,21 and 24 months) Quality of life EQ-5D is a standardized generic instrument for use as a measure of health outcome. Applicable to a wide range of health conditions and treatments, it provides a simple descriptive profile and a single index value for health status.
EQ-5D measures five dimensions of health-related quality of life (HRQOL): mobility, self-care, usual activities, pain/discomfort and anxiety/depression. EQ Visual Analogue Scale: The EQ VAS records the respondent's self-rated health status on a vertically graduated (0-100) visual analogue scale [6]. Economic analysis A cost-effectiveness analysis will be performed alongside the randomized controlled trial. A Markov model will be employed. If the trial reveals no difference in health outcomes or quality of life of the patients, a cost-minimization analysis will be carried out. If we reveal a difference in quality of life between the two groups, we will implement a cost-utility analysis. The economic evaluation will have a health care and societal perspective. Resources used in both treatment arms will be registered prospectively based on reports by the patients and on the hospital patient records. Costs related to consultations at the primary and secondary care level, both at baseline and up to 24 months after randomization, including direct medical costs, indirect costs (production losses), travel costs and patient-/family-related costs will be registered. Quality of life measurements will be collected both at baseline and at several time points during the intervention. A 3% discount rate will be used to discount future costs and benefits.
The cost elements will include costs related to outpatient visits, GP visits, laboratory tests, radiographs and ultrasound, examinations due to suspected stoma complications, treatment of stoma complications, traveling/transportation, and production losses, co-payments and other patient/family expenses. The net costs and outcomes of the two treatment options will be compared and presented as incremental cost-effectiveness ratios.
Sample size Sample size calculations are according to Campbell's [7] and EQ-5D guidelines [8]. Alpha and beta were set at 0.05 and 0.2 respectively and tests were two-sided. We hypothesize that patients followed up by VC will have a minor to moderate increase in the QoL scores. Allowing for a dropout rate of 20%, detecting this difference with confidence we required a total sample size of 170 patients.
Randomization Randomization will be done at the 1-month check-up (baseline) after the patients have given informed consent. The randomization service is web-based and managed by the Norwegian University of Science and Technology.
Patients allocated to VC follow-up may be referred back to surgical clinics at any point in the study. Data gathering Data are being collected for patients in the intervention and the control group in identical ways. QoL and "cost questionnaires" are sent after each follow-up appointment by the patients to the trial center up to 24 months postoperatively. These questionnaires are optically readable, data being consecutively collected in a trial database. SCEs are registered via hospital chart review at 24 months postoperatively. The Norwegian Data Inspectorate has approved the study. All data will be handled with strict confidentiality, and study reports or presentations will maintain the anonymity of patients, surgeons, GPs and hospitals. Data collection will be complete by the end of 2013.
Analysis We will use the intention-to-treat principle when analyzing data. Treatment arms will be compared with respect to potential covariates using continuous and categorical univariable analyses. These will include variables relating to patients (age, sex, comorbidities, cost), treatment (surgical resection, surgical complications), hospital surgical outpatient clinic (cost, patient satisfaction, QoL), VC consultation (cost, patient satisfaction, QoL). The cost elements will include costs related to outpatient visits, VC visits, laboratory tests, radiographs/ultrasound, and examinations due to suspected complications, treatment of complications, traveling/transportation, production losses, co-payments and other patient expenses. The net costs and outcomes of the two treatment/follow-up options will be compared and presented as cost-effectiveness ratios. If the trial reveals no difference in health outcomes or quality of life for the patients, a cost-minimization analysis will be carried out. If we find a difference in quality of life or overall survival rates between the two groups, we will use a cost utility approach. The economic evaluation will have a societal and health care perspective. The method of analysis, including adjusting for covariates will comply with the CONSORT statement [9]. The results will be expressed as odds ratios for binary outcomes, hazard ratios for time- to-event outcomes or mean differences for continuous outcomes with corresponding standard errors, 95% confidence intervals, and associated p-values. P-values will be reported to three decimal places with p-values less than 0.001 reported as p < 0.001. For all tests we will use alpha = 0.05 level of significance.
Ethics The Regional Committee for Medical Research Ethics, North Norway approved this protocol. Patients must provide written consent before entering the trial.
Discussion VC is used as an instrument for follow-up of patients in the postoperative period and for outpatient consultation. From our hospital, we have extensive experience in the use of VC in the follow-up of haemodialysis patients [10] and in dermatology [11, 12]. In addition, a new project has started in the orthopaedic department, where a VC line has been established between the University Hospital and the district medical centre Nordreisa, 155 miles away. In this project, both outpatient patients and postoperative patients are examined by a district orthopaedic nurse under the supervision of an orthopaedic consultant located at the University Hospital. This project has now been organized as a randomised controlled trial, where the primary endpoints are cost-effectiveness and patient satisfaction.
Several articles have reported the use of VC in the follow-up of surgical patients. Wallace et al. aimed to compare joint VC between general practitioners, specialists (surgeons), and patients with standard outpatient referral. This randomised controlled trial showed that allocation of patients to virtual outreach consultations was variably associated with increased offers of follow-up appointments according to site and specialty, but led to significant increases in patients' satisfaction and substantial reductions in tests and investigations. Efficient operation of such services will require appropriate selection of patients, significant service reorganization, and provision of logistical support [13].
A study from Finland investigated the use of VC in the examination of orthopaedic outpatients. VC was found to be feasible and the equipment functioned well technically. The conclusion was that VC between primary and secondary care could be used in the examination of orthopaedic patients whenever no demanding imaging technology was needed [14] Whether VC is cost-effective in the follow-up of surgical patients is debated. The clinical effectiveness and costs of VC in orthopaedics between primary and secondary care were examined in an eight-month prospective comparative study. The general surgery outpatient clinics of two Finnish district hospitals were compared. The direct costs of an outpatient visit were 45% greater per patient than for a VC. A cost-minimization analysis of the alternative interventions showed a net benefit of EU 2,500 in favour of VC [15].
Another Finnish study had similar results. Wider utilization of the VC equipment for other purposes, or the use of less expensive VC equipment, would make services cost saving even at relatively short distances [16].
VC can be used in almost any medical specialty, although the specialties best suited are those with a high visual component. Wound healing and wound management are thus prime candidates for VC follow-up. Development of a suitable telemedical system in this field could have a significant effect on wound care in the community, tertiary referral patterns, and hospital admission rates [5, 17].
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Traditional stoma care | Active comparator | Other: Videoconference stoma careBeing discharged from a hospital with a stoma is a challenge to the patient's quality of life in many aspects. Optimal stoma function and care is essential to keep quality of life best possible. Videoconference can be a useful tool to help patients cope with stoma problems without travelling long distances to a surgical outpatient clinic. |
| Videoconference Stoma Consultations | Experimental | Other: Videoconference stoma careVideoconference Stoma Consultations |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Stoma patients
Key exclusion criteria (2 listed)
- Not able to travel,
- Accepted written consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Videoconference stoma careStoma patients are randomized to videoconference stoma care or surgical outpatients clinic stoma care | Other | Traditional stoma care, Videoconference Stoma Consultations |
Primary outcome
Changes in quality of life
Time frame: up to two years
We aim to compare quality of life measured with EQ-5D questionnaires among patients followed up by VC vs those followed up at the surgical outpatient clinic at 1, 3, 6, 9, 12, 15, 18, 21, 24 months of follow-up. We hypothesize that patients followed up by VC will experience similar or higher scores on quality of life measures during followup.
1 secondary outcome
Cost effectiveness
Time frame: up to two years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jun 2016.
- Background: PubMed 18817503Jarvis-Selinger S, Chan E, Payne R, Plohman K, Ho K. Clinical telehealth across the disciplines: lessons learned. Telemed J E Health. 2008 Sep;14(7):720-5. doi: 10.1089/tmj.2007.0108.
- Background: PubMed 19384459Augestad KM, Lindsetmo RO. Overcoming distance: video-conferencing as a clinical and educational tool among surgeons. World J Surg. 2009 Jul;33(7):1356-65. doi: 10.1007/s00268-009-0036-0.
- Background: PubMed 19390758Doarn CR. The power of video conferencing in surgical practice and education. World J Surg. 2009 Jul;33(7):1366-7. doi: 10.1007/s00268-009-0042-2. No abstract available.
- Background: PubMed 16618327Shannon RJ. Telemedicine in wound healing. Int Wound J. 2005 Sep;2(3):239-40. doi: 10.1111/j.1742-4801.2005.0124b.x. No abstract available.
- Background: PubMed 15192491Wilbright WA, Birke JA, Patout CA, Varnado M, Horswell R. The use of telemedicine in the management of diabetes-related foot ulceration: a pilot study. Adv Skin Wound Care. 2004 Jun;17(5 Pt 1):232-8. doi: 10.1097/00129334-200406000-00012.
- Background: PubMed 10109801EuroQol Group. EuroQol--a new facility for the measurement of health-related quality of life. Health Policy. 1990 Dec;16(3):199-208. doi: 10.1016/0168-8510(90)90421-9.
- Background: PubMed 7580713Campbell MJ, Julious SA, Altman DG. Estimating sample sizes for binary, ordered categorical, and continuous outcomes in two group comparisons. BMJ. 1995 Oct 28;311(7013):1145-8. doi: 10.1136/bmj.311.7013.1145.
- Background: PubMed 10548869Roset M, Badia X, Mayo NE. Sample size calculations in studies using the EuroQol 5D. Qual Life Res. 1999 Sep;8(6):539-49. doi: 10.1023/a:1008973731515.
- Background: PubMed 11323066Moher D, Schulz KF, Altman DG. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet. 2001 Apr 14;357(9263):1191-4.
- Background: PubMed 16035968Rumpsfeld M, Arild E, Norum J, Breivik E. Telemedicine in haemodialysis: a university department and two remote satellites linked together as one common workplace. J Telemed Telecare. 2005;11(5):251-5. doi: 10.1258/1357633054471885.
- Background: PubMed 10925620Moseng D. [Teledermatology--experiences from Northern Norway]. Tidsskr Nor Laegeforen. 2000 Jun 20;120(16):1893-5. Norwegian.
- Background: PubMed 11571079Nordal EJ, Moseng D, Kvammen B, Lochen ML. A comparative study of teleconsultations versus face-to-face consultations. J Telemed Telecare. 2001;7(5):257-65. doi: 10.1258/1357633011936507.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rolv-Ole Lindsetmo, MD, PhD, MPH principal investigator
Institute of Clinical Medicine, Tromsø University, Norway, Univertsity Hospital of North Norway
Questions about this trial
What is this clinical trial studying?
A study testing Videoconference stoma care in people with Surgical Operation With Formation of External Stoma, run by University Hospital of North Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Jun 2016. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in quality of life (time frame: up to two years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01600508, which also lists 18 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jun 2016.