Online Chronic Pain Therapy for Adults
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Purpose
This study will evaluate the usefulness of an online, self-directed treatment for chronic pain that has been designed specifically for individuals who are currently or have previously served in the military.
| Condition | Intervention |
|---|---|
|
Chronic Pain |
Behavioral: Online ABBT for Chronic Pain in Military |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Online Chronic Pain Therapy for Adults |
- Change from baseline in McGill Pain Questionnaire - Short Form [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]A brief self-report questionnaire that measures sensory and affective components of clinical pain.
- Change from baseline in Chronic Pain Acceptance Questionnaire - Revised [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]A 20-item measure of acceptance of chronic pain with items scored from "0 = Never true" to "6 = Always true".
- Change from baseline in Pain Catastrophizing Scale [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]One of the most widely used instruments for measuring catastrophic thinking related to pain. A 13-item measure with items rated from "0 = Not at all" to "4 = All the time."
- Change from baseline in Tampa Scale for Kinesiophobia [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]A self-report measure of fear of movement and/or re-injury. 17 items rated from "1 = strongly disagree" to "4 = strongly agree"
- Change from baseline in Pittsburgh Sleep Quality Index [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]A self-rated questionnaire which assesses sleep quality and disturbances over a 1-month time interval
- Client Satisfaction Questionnaire [ Time Frame: At completion of module, approximately 8 weeks ] [ Designated as safety issue: No ]An eight item questionnaire regarding client satisfaction with the treatment.
- Change from baseline in Beck Depression Inventory - Second Edition [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]A 21 item self-report measure of severity of depressive symptoms.
- Change from baseline in Beck Anxiety Inventory [ Time Frame: 3 months ] [ Designated as safety issue: No ]A 21-item self-report measure assessing severity of symptoms of anxiety
- Change from baseline in PTSD Checklist - Military Version [ Time Frame: 3 months ] [ Designated as safety issue: No ]A 17-item self-report measure assessing severity of PTSD symptoms related to stressful military experiences.
| Estimated Enrollment: | 10 |
| Study Start Date: | June 2012 |
| Estimated Study Completion Date: | March 2013 |
| Estimated Primary Completion Date: | March 2013 (Final data collection date for primary outcome measure) |
-
Behavioral: Online ABBT for Chronic Pain in Military
This study will evaluate the efficacy of an eight-module, online, self-directed treatment for chronic pain using Acceptance-Based Behavioural Therapy (ABBT) as the treatment modality. The online modules are tailored to the unique issues of individuals with a military background. The modules will be delivered via the WebCAPSI Therapy program, an online, password-protected program that allows participants to anonymously progress through all modules at their own pace. ABBT modules cover the following: Introduction, Acceptance, Values, Cognitive Defusion, Mindfulness, Exercise/Pacing/Communication Skills, Self-as-Context, and Willingness. Modules encourage understanding of the information through audio files, military-specific vignettes, written materials, and homework exercises. Modules are designed to be completed in 60 minutes or less. Participants will have access to the online treatment for a three month period and will be encouraged to complete one module per week.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Chronic pain condition of duration 6 months or longer
- Patient at OSI Clinic in Winnipeg
- Access to a computer with internet at least once per week for 60 minutes
Exclusion Criteria:
- Active psychosis
- Actively suicidal
- Unstable living conditions
- Seriously impaired concentration
- Inability to read and write in English
Contacts and Locations| Contact: Pamela L Holens, Ph.D. | (204) 831-3458 | pholens@deerlodge.mb.ca |
| Contact: Kristen Klassen, M.Sc. | (204) 831-3445 | kklassen11@deerlodge.mb.ca |
| Canada, Manitoba | |
| OSI Clinic, Deer Lodge Centre | |
| Winnipeg, Manitoba, Canada, R3J 0L3 | |
| Principal Investigator: | Pamela L Holens, Ph.D. | University of Manitoba |
More Information
No publications provided
| Responsible Party: | University of Manitoba |
| ClinicalTrials.gov Identifier: | NCT01600248 History of Changes |
| Other Study ID Numbers: | H2012:078 |
| Study First Received: | May 10, 2012 |
| Last Updated: | May 14, 2012 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by University of Manitoba:
|
Chronic Pain Military Veteran Online Acceptance |
ClinicalTrials.gov processed this record on May 19, 2013