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Chronic PainNCT03247725

Efficacy of Pain Monitor, a Smartphone App for Chronic Pain

A study testing pain app and Treatment as usual (medical) in people with Chronic Pain, run by Universitat Jaume I at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The present investigation aims at exploring the effect of including a pain app called Pain Monitor for chronic pain patients' daily monitoring. Three conditions will be set: 1. usual treatment (waiting list) 2. usual treatment + app (without alarms) 3. usual treatment + app (with alarms) Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Pain
What is being tested?
pain app and Treatment as usual (medical)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
1 siteSpain
Study dates
1 Sep 2017to 30 Apr 2018
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

  • The patient is over 18 years of age
  • The patient has a mobile phone with Android operating system
  • The patient has the physical ability to use the application
  • The patient does not present psychological and / or cognitive alterations or problems with language that make their participation difficult
  • The patient voluntarily wants to participate and signs the informed consent

Who cannot join

  • The patient is under 18 years
  • The patient does not have a mobile phone or has a mobile phone in which Android is not the operating system (the app is currently only available for Android for economic reasons)
  • The patient does not have the physical capacity to use the application
  • The patient does not have the capacity to participate due to psychological and / or cognitive alterations or problems with language
  • The patient does not want to participate

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Vall d'Hebron Hospital

    Barcelona, 08035

Other trials in Spain

About this study

Official title: Pain Monitor: a Randomized Controlled Trial to Test the Efficacy of a Pain App in the Treatment of Chronic Pain

The present investigation aims at exploring the effect of including a pain app called Pain Monitor for chronic pain patients' daily monitoring. Three conditions will be set:

  1. usual treatment (waiting list)
  2. usual treatment + app (without alarms)
  3. usual treatment + app (with alarms)
Read the detailed description

Chronic pain is defined as one that lasts for at least three to six months, provided that this time is greater than the normal healing period of an injury. This pathology has become an important public health problem due to its high prevalence. In particular, it is estimated that it affects 20-30% of the adult population around the world. Medical interventions are the first-line treatment in recent clinical practice guidelines. Unfortunately, the effectiveness of medical interventions is only modest. Treatments significantly reduce pain on average, but the effect tends to be small . In addition, the drugs are not effective for a large percentage of patients.

What these and other research suggest is that focusing only on large sample studies and the use of average change scores calls into question the usefulness of current patient-centered treatments. As noted by Dr. Turk, when data are averaged, various pain syndromes, drugs, surgical procedures, and studies in different countries are often included, which may mask the efficacy results of different treatments with Different samples. Single case methodology could be one of the ways to overcome these limitations. The single case investigation is a type of experimental study that offers experimental control within a single case.

Some studies have already demonstrated the usefulness of these designs in chronic pain. In fact, the benefits of using this methodology as opposed to large sample studies were discussed recently during the 10th Congress of the European Pain Federation. These benefits include the need for a reduced number of participants, the ability to follow clinical evolution in real time and continuously, the amount of data provided, and applicability when using a control group is impractical or unethical.

The investigators conducting the present investigation recently conducted a study at the Pain Unit of the Vall d'Hebron Hospital to explore the effectiveness of current medical treatments. According to previous investigations, the treatment effect was only small (d = 0.32) and only a percentage of the patients (18.1%) had a clinically significant reduction of pain (ie a reduction greater than 30% ).

From these results and the literature reviewed, a single case design could be an alternative method for research in the Pain Unit. However, the implementation of this type of methodology can be very costly due to the continuous evaluation of the evolution of the patient. In this sense, several studies have already shown that mobile applications (app) can effectively control the evolution of a wide range of pathologies in health settings . In fact, a recent controlled clinical study found that ecological records performed with mobile app had greater reliability than paper-and-pencil records.

Rosser and Eccleston conducted a comprehensive review of existing apps for pain and the conclusion was that there was little evidence to support the use of current apps. Specifically, these authors showed that most apps did not specify whether their content was validated, did not include psychological components and none had been applied in a clinical study. In light of these results, Dr. Carlos Suso Ribera and Dr. Ribera Canudas contacted the research team Labpsitec of Jaume I University, who were developing an application for pain called "Pain Monitor". Dr. Carlos Suso Ribera and Dr. Ribera Canudas of the Pain Unit collaborated with Dr. Azucena García Palacios and Dr. Diana Castilla López of the Universitat Jaume I in the final development of the application of pain, Following the guidelines of Rosser and Eccleston.

App content validity and usability was tested in a previous study at the pain unit of the Vall d'Hebron Hospital (Suso-Ribera et al., in preparation). Thus, the study objective is to test if the introduction of this tool in the day-to-day work of the pain unit improves pain management of chronic pain patients. To do this, it is necessary to compare the evolution of patients who follow the usual treatment at the pain unit (without app) with a group of patients who do use the Pain Monitor app. In addition, the present study investigators have created a new utility that allows alarms to be generated by healthcare professionals in the presence of an undesired event, such as an adverse effect of the medication or a lack of response to medical treatment. Before determining that both the use of the app and this new utility (alarms) are beneficial for patient care, it is necessary to perform a clinical trial comparing the 3 conditions mentioned above:

  1. usual treatment (waiting list)
  2. usual treatment + app (without alarms)
  3. usual treatment + app (with alarms) Therefore, this is a clinical trial without drugs. This is not an observational study since the physicians of patients in the app + alarms condition will be asked to react to an alarm (i.e., if the patient has nausea for 3 consecutive days) by calling the patient and changing the treatment telematically, if necessary, so that the patient can collect the prescription at his primary care center.

If the condition app with alarms results in a better treatment of chronic pain patients, participants of the other two conditions will be offered the possibility to use the app with alarms at the end of the study.

The study will be conducted at the Pain Unit of the Vall d'Hebron Hospital. All study procedures have been approved by the ethical committee of the Vall d'Hebron Hospital.

Conditions
Chronic Pain
Being tested
pain app, Treatment as usual (medical)
Medical subject headings
Chronic Pain

What participants receive

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

  • pain appOther

    Pain Monitor app has been developed by a multidisciplinary pain expert panel, including physicians, psychologists, and nurses. Content has been validated in a previous study and usability has been shown to be excellent.

  • Treatment as usual (medical)Other

    Patients will be offered the usual treatment for their pain, which is not changed by study participation

Study groups in NCT03247725
Study groupRoleWhat they receive
Treatment as usual (waiting list)Active comparatorPatients at this condition will receive the usual medical treatment at the pain unit, but they will not be monitored daily using the app.
Receives: Other: Treatment as usual (medical)
Treatment as usual + app (without alarm)ExperimentalParticipants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Because alarms will not be generated, physicians will not know if an undesired event is occuring despite the app is actually collecting data.
Receives: Other: pain app; Other: Treatment as usual (medical)
Treatment as usual + app (with alarm)ExperimentalParticipants at this condition will receive the usual medical treatment for their pain but also they will be monitored daily using the Pain Monitor app. Alarms will be generated in the face of certain preestablished events. Physicians will be asked to call patients and change/stop treatment if an alarm is received.
Receives: Other: pain app; Other: Treatment as usual (medical)

What is being measured

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

  1. Change in pain intensity

    A numerical rating scale (0-10 range) will be used.

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  2. Change in side effects

    A list of the most frequent side effects of pain medication was created

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  3. Change in pain intensity

    A numerical rating scale (0-10 range) will be used.

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  4. Change in side effects

    A list of the most frequent side effects of pain medication was created

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

Secondary outcomes (14)
  1. Change in mood

    Questionnaire on mood validated against the Profile of Mood States

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  2. Change in mood

    Questionnaire on mood validated against the Profile of Mood States

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  3. Change in rescue medication use

    Amount of rescue medication will be assessed

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  4. Change in rescue medication use

    Amount of rescue medication will be assessed

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  5. Change in pain interference

    Interference of pain with patient's life

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  6. Change in pain interference

    Interference of pain with patient's life

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  7. Change in general health

    A general health item was validated against the phsyical health scale of the Short Form 12

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  8. Change in general health

    A general health item was validated against the phsyical health scale of the Short Form 12

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  9. Change in fear of pain

    2 items validated against the Fear Avoidance Beliefs Scale

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  10. Change in fear of pain

    2 items validated against the Fear Avoidance Beliefs Scale

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  11. Change in pain acceptance

    2 items validated against the Chronic Pain Acceptance Questionnaire

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  12. Change in pain acceptance

    2 items validated against the Chronic Pain Acceptance Questionnaire

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

  13. Change in pain catastrophizing

    3 items validated against the Pain Catastrophizing Scale

    Measured: Dialy during 30 days (app condition) in the app condition (with and without alarm)

  14. Change in pain catastrophizing

    3 items validated against the Pain Catastrophizing Scale

    Measured: Twice (first day of study and 30 days after, at the end of study) in the TAU condition

Timeline

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

  1. First posted14 Aug 2017
  2. Study start1 Sep 2017
  3. Primary completion30 Mar 2018
  4. Study completion30 Apr 2018

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Three conditions. Patients will be randomly assigned to one of the three conditions.
Masking
None (open label)
Enrolment
150 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03247725
Sponsor's protocol ID
UJI_PainMonitor
Status last verified
May 2018
First submitted
25 Jul 2017
Last updated
17 May 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Only the two principal investigators, Dr. Mesas and Dr. Suso, will be able to access to individual participant data.

Publications

  • Rosser BA, Eccleston C. Smartphone applications for pain management. J Telemed Telecare. 2011;17(6):308-12. doi: 10.1258/jtt.2011.101102. Epub 2011 Aug 15.

    PubMed 21844177
  • Suso-Ribera C, Mesas A, Medel J, Server A, Marquez E, Castilla D, Zaragoza I, Garcia-Palacios A. Improving pain treatment with a smartphone app: study protocol for a randomized controlled trial. Trials. 2018 Feb 27;19(1):145. doi: 10.1186/s13063-018-2539-1.

    PubMed 29482614

Questions about this trial

What is this clinical trial studying?

A study testing pain app and Treatment as usual (medical) in people with Chronic Pain, run by Universitat Jaume I at 1 site in Spain.

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 5 inclusion and 5 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 May 2018. 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 Spain. 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?

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?

Change in pain intensity (time frame: Dialy during 30 days (app condition) in the app condition (with and without alarm)). The study lists 4 primary outcomes in all. 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 NCT03247725, which also lists 2 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 May 2018.

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