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Efficacy of Pain Monitor, a Smartphone App for Chronic Pain

Primary Purpose

Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
pain app
Treatment as usual (medical)
Sponsored by
Universitat Jaume I
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Sites / Locations

  • Vall d'Hebron Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Treatment as usual (waiting list)

Treatment as usual + app (without alarm)

Treatment as usual + app (with alarm)

Arm Description

Patients at this condition will receive the usual medical treatment at the pain unit, but they will not be monitored daily using the app.

Participants 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.

Participants 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.

Outcomes

Primary Outcome Measures

Change in pain intensity
A numerical rating scale (0-10 range) will be used.
Change in side effects
A list of the most frequent side effects of pain medication was created
Change in pain intensity
A numerical rating scale (0-10 range) will be used.
Change in side effects
A list of the most frequent side effects of pain medication was created

Secondary Outcome Measures

Change in mood
Questionnaire on mood validated against the Profile of Mood States
Change in mood
Questionnaire on mood validated against the Profile of Mood States
Change in rescue medication use
Amount of rescue medication will be assessed
Change in rescue medication use
Amount of rescue medication will be assessed
Change in pain interference
Interference of pain with patient's life
Change in pain interference
Interference of pain with patient's life
Change in general health
A general health item was validated against the phsyical health scale of the Short Form 12
Change in general health
A general health item was validated against the phsyical health scale of the Short Form 12
Change in fear of pain
2 items validated against the Fear Avoidance Beliefs Scale
Change in fear of pain
2 items validated against the Fear Avoidance Beliefs Scale
Change in pain acceptance
2 items validated against the Chronic Pain Acceptance Questionnaire
Change in pain acceptance
2 items validated against the Chronic Pain Acceptance Questionnaire
Change in pain catastrophizing
3 items validated against the Pain Catastrophizing Scale
Change in pain catastrophizing
3 items validated against the Pain Catastrophizing Scale

Full Information

First Posted
July 25, 2017
Last Updated
May 16, 2018
Sponsor
Universitat Jaume I
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1. Study Identification

Unique Protocol Identification Number
NCT03247725
Brief Title
Efficacy of Pain Monitor, a Smartphone App for Chronic Pain
Official Title
Pain Monitor: a Randomized Controlled Trial to Test the Efficacy of a Pain App in the Treatment of Chronic Pain
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
March 30, 2018 (Actual)
Study Completion Date
April 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitat Jaume I

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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: usual treatment (waiting list) usual treatment + app (without alarms) usual treatment + app (with alarms)
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: usual treatment (waiting list) usual treatment + app (without alarms) 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three conditions. Patients will be randomly assigned to one of the three conditions.
Masking
None (Open Label)
Masking Description
Patients will be informed of the condition they have been assigned to.
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment as usual (waiting list)
Arm Type
Active Comparator
Arm Description
Patients at this condition will receive the usual medical treatment at the pain unit, but they will not be monitored daily using the app.
Arm Title
Treatment as usual + app (without alarm)
Arm Type
Experimental
Arm Description
Participants 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.
Arm Title
Treatment as usual + app (with alarm)
Arm Type
Experimental
Arm Description
Participants 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.
Intervention Type
Other
Intervention Name(s)
pain app
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Treatment as usual (medical)
Intervention Description
Patients will be offered the usual treatment for their pain, which is not changed by study participation
Primary Outcome Measure Information:
Title
Change in pain intensity
Description
A numerical rating scale (0-10 range) will be used.
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in side effects
Description
A list of the most frequent side effects of pain medication was created
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in pain intensity
Description
A numerical rating scale (0-10 range) will be used.
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in side effects
Description
A list of the most frequent side effects of pain medication was created
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Secondary Outcome Measure Information:
Title
Change in mood
Description
Questionnaire on mood validated against the Profile of Mood States
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in mood
Description
Questionnaire on mood validated against the Profile of Mood States
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in rescue medication use
Description
Amount of rescue medication will be assessed
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in rescue medication use
Description
Amount of rescue medication will be assessed
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in pain interference
Description
Interference of pain with patient's life
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in pain interference
Description
Interference of pain with patient's life
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in general health
Description
A general health item was validated against the phsyical health scale of the Short Form 12
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in general health
Description
A general health item was validated against the phsyical health scale of the Short Form 12
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in fear of pain
Description
2 items validated against the Fear Avoidance Beliefs Scale
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in fear of pain
Description
2 items validated against the Fear Avoidance Beliefs Scale
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in pain acceptance
Description
2 items validated against the Chronic Pain Acceptance Questionnaire
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in pain acceptance
Description
2 items validated against the Chronic Pain Acceptance Questionnaire
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition
Title
Change in pain catastrophizing
Description
3 items validated against the Pain Catastrophizing Scale
Time Frame
Dialy during 30 days (app condition) in the app condition (with and without alarm)
Title
Change in pain catastrophizing
Description
3 items validated against the Pain Catastrophizing Scale
Time Frame
Twice (first day of study and 30 days after, at the end of study) in the TAU condition

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ángela Mesas Idáñez, MD
Organizational Affiliation
Staff Doctor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vall d'Hebron Hospital
City
Barcelona
ZIP/Postal Code
08035
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Only the two principal investigators, Dr. Mesas and Dr. Suso, will be able to access to individual participant data.
Citations:
PubMed Identifier
21844177
Citation
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.
Results Reference
background
PubMed Identifier
29482614
Citation
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.
Results Reference
derived

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Efficacy of Pain Monitor, a Smartphone App for Chronic Pain

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