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Musculoskeletal DiseasesNCT06130098

Investıgatıon Of The Effect Of Traınıng And Counselıng Provıded By Tele Nursing

A study testing experimental group in people with Musculoskeletal Diseases, run by Hasan Kalyoncu University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

To examine the effect of education and consultancy provided via telenursing service after total knee arthroplasty on postoperative quality of life and some complications. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Musculoskeletal Diseases
What is being tested?
experimental group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
72 participants
Where
1 siteTurkey (Türkiye)
Study dates
13 Nov 2023to 30 Dec 2024
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 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Having TDP surgery for the first time,
  • Having primary elective TKA surgery,
  • Having had a single (unilateral) knee prosthesis surgery,
  • Patients whose FFP indication is osteoarthritis,
  • No hearing, understanding, vision or speaking problems,
  • Agreeing to participate in the research voluntarily,
Show all 11Show fewer
  • Able to understand and speak Turkish,
  • Least literate,
  • Those who have a mobile phone that can take photos of themselves or those nearby,
  • Patients who have a smartphone or a smartphone nearby,
  • Patients who do not develop serious complications that will delay discharge from the hospital

Who cannot join

  • Answering data collection forms incompletely
  • Being illiterate in Turkish
  • Patients who agreed to participate in the study but later left
  • Patients who cannot be reached when called and whose follow-up cannot be completed

Trial locations and contacts

1 site in 1 country.

GULSAH BEKTAS, LECTURER contact

+905513846382

bektasgulsah@yahoo.com.tr

Turkey (Türkiye)1 site
  • Nevşehir Devlet Hastanesi

    Nevşehir, Merkez, 50000

    GULSAH BEKTAS, LECTURER, +905513846382, bektasgulsah@yahoo.com.tr

Other trials in Turkey (Türkiye)

About this study

Official title: Investıgatıon Of The Effect Of Traınıng And Counselıng Provıded By Tele Nursıng Servıce After Total Knee Prosthesıs On Post-Operatıve Qualıty Of Lıfe And Complıcatıons

To examine the effect of education and consultancy provided via telenursing service after total knee arthroplasty on postoperative quality of life and some complications.

Read the detailed description

It is estimated that osteoarthritis, which causes low quality of life in old age and is one of the serious obstacles to physical independence, affects more than 250 million people in the world, as the elderly population in the world and in our country increases. Osteoarthritis is characterized by degeneration of joint cartilage, accompanied by pain and loss of function, and its etiology is not yet fully known; It is a chronic joint disease that is accompanied by metabolic, genetic and other affecting factors.

The most common area of osteoarthritis is the knees, and its progression is generally slow. Knee osteoarthritis is a public health problem due to increasing age, obesity and the increase in knee traumas. Knee osteoarthritis begins to occur at the age of 40 and is estimated to be more common in women than in men. According to World Health Organization (WHO) data, osteoarthritis is seen at a rate of 18% in women aged 60 and over and 9.6% in men (6). It has been stated that the prevalence of osteoarthritis increases as the elderly population increases in the USA, and 62% of osteoarthritis patients in New Zealand have knee osteoarthritis. According to the Health Survey data conducted by the Turkish Statistical Institute (TUIK) (2019) in our country, it is stated that 11.2% of the population has problems related to osteoarthritis.

Knee osteoarthritis is a disease with multiple etiologies consisting of regional and systemic factors. There are modifiable and non-modifiable risk factors such as age, gender, nutrition, genetics, obesity, trauma, alignment disorders, occupation, physical activity, and muscle weakness. In the treatment of knee osteoarthritis, total knee prosthesis (TKA) is applied to patients when conservative approaches such as medical and physical therapy are insufficient and surgical interventions such as osteotomy and debridement fail to yield results. TDP; It is the process of replacing the damaged joint surface (tibial, femoral, patellar joint surfaces) in the knee, which develops due to osteoarthritis, rheumatoid arthritis, post-traumatic arthritis and other nonspecific arthritis, with metal or polyethylene prostheses. The purpose of total knee prosthesis is; It is applied to increase knee joint functions, correct deformities, reduce pain, and also improve the quality of life of individuals.

Patients who undergo TKA surgery are generally in the elderly group. In this group, patients with chronic diseases (atherosclerotic heart disease, hypertension, diabetes mellitus, chronic obstructive lung), those who have previously undergone orthopedic surgery, long-term surgery, inappropriate prosthesis selection for the individual, metabolic problems, soft tissue problems, problems in bone tissue and prosthesis design. Errors in application technique increase the risk of morbidity and mortality before, during and after TKA surgery.

Since FFP surgery is a major orthopedic surgical intervention, it can lead to serious complications. These complications; Complications related to the wound site include neurovascular complications (deep vein thrombosis, pulmonary embolism), infection (superficial infection, deep infection), patellafemoral problems, instability, joint stiffness, early aseptic loosening, osteolysis and periprosthetic fracture formation. Especially in case of serious complications such as aseptic loosening, infection and pain, the patient cannot use the prosthesis and revision may be required.

Nurses working in the field of orthopedics have an important role in reducing/preventing complications and re-surgeries related to TKA surgery, increasing patient satisfaction and reducing care costs. Basic principles of orthopedic nursing in patients who will undergo TKA surgery; It includes preventing possible complications, ensuring the functionality of the knee and preserving mobilization. At the same time, orthopedic nurses should give detailed counseling to patients, starting from the preoperative period, about preoperative preparation, surgical procedure, postoperative care, home care after discharge (medication use, exercise, nutrition, wound care, etc.), complications that may develop and initiatives to prevent them. . The advisory role of the nursing profession; It is expected that the society will recognize and use its own opportunities and resources regarding protecting and improving public health, increasing the quality of life, coping with disease-related problems, and ensuring that patients have access to scientific information. Effective counseling carried out by the nurse; It accelerates recovery and facilitates the adaptation of the patient and his family to the process.

Today, patients are discharged early after surgery due to the insufficient number of beds in hospitals, the cost of long-term stays, and the increased risk of infection. Early discharge can turn into a troublesome process for the patient and his family. Because many patients cannot adequately prepare for the post-operative recovery period at home, they feel inadequate and insecure during this process, and their recovery period can last up to a month.

Being tested
control group, experimental group
Keywords
total knee replacement, telenursing, post-discharge care
Medical subject headings
Musculoskeletal Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • control groupOther

    Training by the clinical nurse before discharge. Prepare an educational brochure and give it to patients. Application of patient information form, EQ-5D-5L Quality of Life and OKS Scale During the routine check-up in the first week, evaluates the development of complications without knowing which group the patient is in.

    Within the first week and at the end of the fourth week, the wound site is evaluated by the physician for the development of complications, . Patients who cannot come for a check-up should send a photo of the wound area to the researcher via WhatsApp application, and the photo will be forwarded to the clinician who performed the surgery and the physician will record the complication situation. It is planned to receive complication development and wound site evaluation results from the physician system.

    At the end of the fourth and sixth weeks after discharge, the EQ-5D-5L and OKS scale must be filled in again by the patients.

  • experimental groupOther

    Providing training before discharge Prepare an educational brochure and give it to patients. You will be contacted by phone at the end of the first, second, third and fourth weeks after discharge.

    Application of patient information form, EQ-5D-5L Quality of Life and OKS Scale Evaluating the wound site in terms of complications within the first week and at the end of the fourth week. It is planned to receive complication development and wound site evaluation results from the system.

    After the first check-up, calling the patients in the study group at the end of the first week after discharge.

    Providing training on the subjects included in the training brochure in the first phone call and recording any existing problems.

    In the fourth meeting, tele-nursing service will be provided through the "Telephone Counseling Protocol".

    EQ-5D-5L and OKS forms must be filled out again by patients at the routine check-up at the end of the fourth and sixth weeks after discharge.

Study groups in NCT06130098
Study groupRoleWhat they receive
control groupActive comparatorTraining by the clinical nurse before discharge. Prepare an educational brochure and give it to patients. Application of patient information form, EQ-5D-5L Quality of Life and Oxford Knee Score Scale During the routine check-up in the first week, evaluates the development of complications without knowing which group the patient is in. Within the first week and at the end of the fourth week, the wound site is evaluated by the physician for the development of complications, . Patients who cannot come for a check-up should send a photo of the wound area to the researcher via WhatsApp application, and the photo will be forwarded to the clinician who performed the surgery and the physician will record the complication situation. It is planned to receive complication development and wound site evaluation results from the physician system. At the end of the fourth and sixth weeks after discharge, the EQ-5D-5L and OKS scale must be filled in again by the patients.
Receives: Other: control group
experimental groupActive comparatorActive Comparator: experimental group Providing education to patients by preparing a pre-discharge education brochure. You will be contacted by phone at the end of the first, second, third and fourth weeks after discharge. Application of the patient information form, EQ-5D-5L Quality of Life and Oxford Knee Score Scale. Evaluation of the wound site in terms of complications at the end of the first and fourth weeks. It is planned to receive complication development and wound site evaluation results from the system. After the first check-up, a call is made at the end of the first week after discharge. Providing training on the subjects included in the training brochure during the first phone call In the fourth meeting, tele-nursing service was provided through the "Telephone Counseling Protocol" Refilling of the EQ-5D-5L quality of life and Oxford Knee Score scale by patients at routine check-up at the end of the fourth and sixth weeks after discharge
Receives: Other: experimental group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. OXFORD KNEE SCORE

    To evaluate the gains in daily life and the change in the health of patients who haveundergone TKA surgery after surgery.The scoring system is a 12-item self-reported measurement tool to evaluate physical function and pain in patients with total knee arthroplasty. After this scoring system is applied, the answers given by the patients are scored between 0 and 4. In total, a patient can get a minimum of 0 and a maximum of 48 points. For results, 0-19 points are considered excellent, 20-29 points are good, 30-39 points are fair, and 40-48 points are considered poor.

    Measured: at the end of the fourth and sixth weeks

Secondary outcomes (1)
  1. EQ-5D-5L quality of life scale

    To evaluate the quality of life.It consists of two parts. The first part is the health profile of that day; It allows it to be defined in five sub-dimensions: movement, self-care, usual activities, pain / discomfort and anxiety / depression. Answers given in each section; It has 5 options: "no problem", "mild problem", "moderate problem", "severe problem" and "extreme problem". The second part consists of the visual analog scale (VAS). In this section, individuals give values between 0 and 100 about their current health status and mark it on a thermometer-like scale. Quality of life scores ranging from 0 to 100 are obtained from the visual analog scale section. As the score of the scale increases, the perception of health increases positively.

    Measured: at the end of the fourth and sixth weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Nov 2023
  2. Study start13 Nov 2023 (estimated)
  3. Primary completion30 Nov 2024 (estimated)
  4. Study completion30 Dec 2024 (estimated)

Resources

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
There are two groups: control and study groups. Certain applications were planned to be applied to the control group and the study group.
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
72 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06130098
Sponsor's protocol ID
HasanKU-HEM-GB-01
Status last verified
Nov 2023
First submitted
6 Nov 2023
Last updated
13 Nov 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing experimental group in people with Musculoskeletal Diseases, run by Hasan Kalyoncu University at 1 site in Turkey (Türkiye).

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 11 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 13 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact GULSAH BEKTAS, LECTURER (+905513846382, bektasgulsah@yahoo.com.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

OXFORD KNEE SCORE (time frame: at the end of the fourth and sixth weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 13 Nov 2023.

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