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Living Well With Chronic Pain (EPIO)

Primary Purpose

Chronic Pain, Widespread

Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
EPIO
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Pain, Widespread focused on measuring Pain, Chronic Pain, Self-management, E-health, Appication, App, Intervention, Cognitive Behavioral Therapy, CBT, Acceptance and Commitment Therapy, ACT, Psychological well-being

Eligibility Criteria

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

Inclusion Criteria:

  • Chronic pain (pain > 3 months)
  • > 18 years of age
  • Able to write/read/speak Norwegian
  • Have their own smart phone, PC or tablet

Exclusion Criteria:

  • Cancer related pain
  • Migraine

Sites / Locations

  • Oslo University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

No Intervention

Active Comparator

Arm Label

EPIO (e-health intervention)

treatment as usual

Experimental without introduction group and follow up phone calls

Arm Description

Participants will get access to one module every third day (total 9 modules). The app consists of cognitive behavioral pain self-management material, including educational material and relaxation training exercises.

Participants will get treatment as usual during the study. All participants will get access to the app after ended study if interested.

One extra arm (non randomized) has been included to examine whether participants who receive the EPIO intervention without receiving an introduction session and follow up phone calls will still describe benefiting from the receiving the intervention

Outcomes

Primary Outcome Measures

Brief Pain Inventory (BPI) (Short Form) - Assessing change
9 item scale measuring pain interference on function. Using this measure, respondents rate their worst, least, average, and current pain intensity and also rate the degree to which pain interferes with 7 domains of functioning (general activity, mood, walking ability, normal work, relations with other persons, sleep, and enjoyment of life) on a scale of 0 to 10. There is no scoring algorithm, but "worst pain" or the arithmetic mean of the four severity items can be used as measures of pain severity; the arithmetic mean of the seven interference items can be used as a measure of pain interference.

Secondary Outcome Measures

Pain Catastrophizing Scale (PCS) - Assessing change
13 item scale measuring helplessness, magnification and rumination. Patients rate items on a scale from 0 (not at all) to 4 (all the time). The total score range for the PCS is 0 to 52, with higher scores reflecting higher degrees of catastrophizing.
Chronic Pain Acceptance Questionnaire (CPAQ) - Assessing change
8 item scale measuring pain acceptance. It is scored on a 7-point Likert scale (0 = never true; 6 = always true). Higher scores reflect higher acceptance of pain.
Self-Regulatory Fatigue 18 (SRF-18) - Assessing change
18 item scale measuring self-regulatory capacity with cognitive, emotional, and behavioral components. Items are scored on a 5-point Likert scale (1 to 5). The obtainable score range is 18 to 90, with higher numbers reflecting higher SRF.
The Hospital Anxiety and Depression Scale (HADS) - Assessing change
14 item scale measuring anxiety and depression. Respondents are asked to indicate which of 4 response options (rated from 0-3; score range, 0-42) comes closest to describing how they have been feeling in the previous week for each item. Scores from 0-7 on the subscales are regarded as being in the normal range; a score of 11 or higher indicates a probable presence of a mood disorder, and a score of 8-10 is suggestive of the presence of the state.
System Usability Scale (SUS)
1o item scale measuring usability, with five response options for respondents; from Strongly agree to Strongly disagree. The obtainable score range is 25 to 100. A SUS score above a 68 would be considered above average and anything below 68 is below average.
RAND Health Related Quality of Life - Assessing change
36 item scale measuring health related quality of life. The RAND-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability.

Full Information

First Posted
September 20, 2018
Last Updated
January 4, 2023
Sponsor
Oslo University Hospital
Collaborators
The Research Council of Norway, University of Oslo, University College of Southeast Norway, Diakonhjemmet Hospital, Vestre Viken Hospital Trust, Drammen municipality, Norway, Mayo Clinic, University of Twente, University of Washington, University of Florida
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1. Study Identification

Unique Protocol Identification Number
NCT03705104
Brief Title
Living Well With Chronic Pain
Acronym
EPIO
Official Title
Living Well With Chronic Pain: Using Person-centered E-health Design to Support Self-management
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 3, 2019 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
January 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
The Research Council of Norway, University of Oslo, University College of Southeast Norway, Diakonhjemmet Hospital, Vestre Viken Hospital Trust, Drammen municipality, Norway, Mayo Clinic, University of Twente, University of Washington, University of Florida

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 goal of this project is to test the effect of an interactive e-health intervention for people with chronic pain.
Detailed Description
Chronic pain conditions are common and difficult to cure. As much as 30% of adults in Norway experience moderate-to-severe chronic pain, i.e., pain having lasted more than 3 months. Chronic pain is also the most common cause of sick leave and disability pension in Norway. Despite a clear request from the authorities, e-health interventions for chronic pain has not yet been tested and implemented. The aim of this study is to investigate the effect of an interactive e-health intervention for people living with chronic pain, using outcome measures such as pain intensity, pain acceptance, anxiety/depression and quality of life. The e-health intervention will first be tested in a pilot study with 50 patients with different pain diagnoses and eventually in a randomized controlled trial with a sample of 240 patients with different pain diagnoses. The intervention will consist of one face-to-face introductory group followed by 9 app-based modules containing cognitive behavioral pain self-management material. The 9 modules will be distributed over minimum 27 days (minimum 3 days per module). The participants in the randomized controlled trial will be randomly assigned to use the e-health intervention or to a treatment as usual control group. Both groups will receive outcome measures to complete at baseline and at 3, 6 and 12 months. Post-RCT, the EPIO study will also include a non-randomized group receiving the app-based EPIO program but without receiving an introduction session and follow up phone calls to examine potential benefits from receiving the app-based program only.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain, Widespread
Keywords
Pain, Chronic Pain, Self-management, E-health, Appication, App, Intervention, Cognitive Behavioral Therapy, CBT, Acceptance and Commitment Therapy, ACT, Psychological well-being

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
340 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EPIO (e-health intervention)
Arm Type
Experimental
Arm Description
Participants will get access to one module every third day (total 9 modules). The app consists of cognitive behavioral pain self-management material, including educational material and relaxation training exercises.
Arm Title
treatment as usual
Arm Type
No Intervention
Arm Description
Participants will get treatment as usual during the study. All participants will get access to the app after ended study if interested.
Arm Title
Experimental without introduction group and follow up phone calls
Arm Type
Active Comparator
Arm Description
One extra arm (non randomized) has been included to examine whether participants who receive the EPIO intervention without receiving an introduction session and follow up phone calls will still describe benefiting from the receiving the intervention
Intervention Type
Behavioral
Intervention Name(s)
EPIO
Other Intervention Name(s)
e-health intervention for chronic pain
Intervention Description
App for self-management of chronic pain An app consisting of 9 modules focusing on cognitive behavioral pain self-management.
Primary Outcome Measure Information:
Title
Brief Pain Inventory (BPI) (Short Form) - Assessing change
Description
9 item scale measuring pain interference on function. Using this measure, respondents rate their worst, least, average, and current pain intensity and also rate the degree to which pain interferes with 7 domains of functioning (general activity, mood, walking ability, normal work, relations with other persons, sleep, and enjoyment of life) on a scale of 0 to 10. There is no scoring algorithm, but "worst pain" or the arithmetic mean of the four severity items can be used as measures of pain severity; the arithmetic mean of the seven interference items can be used as a measure of pain interference.
Time Frame
Baseline, and at 3, 6, and 12 months.
Secondary Outcome Measure Information:
Title
Pain Catastrophizing Scale (PCS) - Assessing change
Description
13 item scale measuring helplessness, magnification and rumination. Patients rate items on a scale from 0 (not at all) to 4 (all the time). The total score range for the PCS is 0 to 52, with higher scores reflecting higher degrees of catastrophizing.
Time Frame
Baseline, and at 3, 6, and 12 months.
Title
Chronic Pain Acceptance Questionnaire (CPAQ) - Assessing change
Description
8 item scale measuring pain acceptance. It is scored on a 7-point Likert scale (0 = never true; 6 = always true). Higher scores reflect higher acceptance of pain.
Time Frame
Baseline, and at 3, 6, and 12 months.
Title
Self-Regulatory Fatigue 18 (SRF-18) - Assessing change
Description
18 item scale measuring self-regulatory capacity with cognitive, emotional, and behavioral components. Items are scored on a 5-point Likert scale (1 to 5). The obtainable score range is 18 to 90, with higher numbers reflecting higher SRF.
Time Frame
Baseline, and at 3, 6, and 12 months.
Title
The Hospital Anxiety and Depression Scale (HADS) - Assessing change
Description
14 item scale measuring anxiety and depression. Respondents are asked to indicate which of 4 response options (rated from 0-3; score range, 0-42) comes closest to describing how they have been feeling in the previous week for each item. Scores from 0-7 on the subscales are regarded as being in the normal range; a score of 11 or higher indicates a probable presence of a mood disorder, and a score of 8-10 is suggestive of the presence of the state.
Time Frame
Baseline, and at 3, 6, and 12 months.
Title
System Usability Scale (SUS)
Description
1o item scale measuring usability, with five response options for respondents; from Strongly agree to Strongly disagree. The obtainable score range is 25 to 100. A SUS score above a 68 would be considered above average and anything below 68 is below average.
Time Frame
At 3 months
Title
RAND Health Related Quality of Life - Assessing change
Description
36 item scale measuring health related quality of life. The RAND-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability.
Time Frame
Baseline, and at 3, 6, and 12 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic pain (pain > 3 months) > 18 years of age Able to write/read/speak Norwegian Have their own smart phone, PC or tablet Exclusion Criteria: Cancer related pain Migraine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lise Solberg Nes, PhD
Organizational Affiliation
Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35488295
Citation
Bostrom K, Varsi C, Eide H, Borosund E, Kristjansdottir OB, Schreurs KMG, Waxenberg LB, Weiss KE, Morrison EJ, Nordang EF, Stubhaug A, Nes LS. Engaging with EPIO, a digital pain self-management program: a qualitative study. BMC Health Serv Res. 2022 Apr 29;22(1):577. doi: 10.1186/s12913-022-07963-x.
Results Reference
derived
PubMed Identifier
35293866
Citation
Eiken AG, Nordanger DO, Solberg Nes L, Varsi C. Patients' Experiences of Using an eHealth Pain Management Intervention Combined With Psychomotor Physiotherapy: Qualitative Study. JMIR Form Res. 2022 Mar 16;6(3):e34458. doi: 10.2196/34458.
Results Reference
derived
PubMed Identifier
33766028
Citation
Varsi C, Ledel Solem IK, Eide H, Borosund E, Kristjansdottir OB, Heldal K, Waxenberg LB, Weiss KE, Schreurs KMG, Morrison EJ, Stubhaug A, Solberg Nes L. Health care providers' experiences of pain management and attitudes towards digitally supported self-management interventions for chronic pain: a qualitative study. BMC Health Serv Res. 2021 Mar 25;21(1):275. doi: 10.1186/s12913-021-06278-7.
Results Reference
derived
PubMed Identifier
33094734
Citation
Bostrom K, Borosund E, Varsi C, Eide H, Flakk Nordang E, Schreurs KM, Waxenberg LB, Weiss KE, Morrison EJ, Cvancarova Smastuen M, Stubhaug A, Solberg Nes L. Digital Self-Management in Support of Patients Living With Chronic Pain: Feasibility Pilot Study. JMIR Form Res. 2020 Oct 23;4(10):e23893. doi: 10.2196/23893.
Results Reference
derived
PubMed Identifier
31961331
Citation
Ledel Solem IK, Varsi C, Eide H, Kristjansdottir OB, Borosund E, Schreurs KMG, Waxenberg LB, Weiss KE, Morrison EJ, Haaland-Overby M, Bevan K, Zangi HA, Stubhaug A, Solberg Nes L. A User-Centered Approach to an Evidence-Based Electronic Health Pain Management Intervention for People With Chronic Pain: Design and Development of EPIO. J Med Internet Res. 2020 Jan 21;22(1):e15889. doi: 10.2196/15889.
Results Reference
derived
PubMed Identifier
30877780
Citation
Ledel Solem IK, Varsi C, Eide H, Kristjansdottir OB, Mirkovic J, Borosund E, Haaland-Overby M, Heldal K, Schreurs KM, Waxenberg LB, Weiss KE, Morrison EJ, Solberg Nes L. Patients' Needs and Requirements for eHealth Pain Management Interventions: Qualitative Study. J Med Internet Res. 2019 Apr 1;21(4):e13205. doi: 10.2196/13205.
Results Reference
derived
Links:
URL
http://epio.no
Description
Study web page

Learn more about this trial

Living Well With Chronic Pain

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