Chronic Pain Clinical Trial
Official title:
Evaluation of a Mind-body Based Application for the Treatment of Chronic/Persistent Pain.
Verified date | November 2022 |
Source | University of the Fraser Valley |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
We are investigating the effects of a mind-body based mobile application on the experience of chronic pain. Participants meeting our criteria for chronic pain (confirmed via self-report) will complete an online baseline questionnaire. Eligible participants will be enrolled in the study and randomized into control (usual care, waitlisted) or intervention group (6-week mind-body based mobile application intervention). Randomization will be stratified by pain intensity and gender using computer-generated block randomization to create varying block sizes of 4 and 8. We will run the trial in multiple cohorts in series to obtain desired sample size. All participants will complete online questionnaires at baseline and post-intervention at 6 weeks that measure pain intensity, interference with daily living, pain perceptions, mental health outcomes, and medication use. Participants will also complete weekly questionnaires on weeks 2 to 6 to gauge frequency of application usage (intervention) or other pain treatments (control). Participants in the intervention group will be asked to repeat the follow-up questionnaire at 12-weeks.
Status | Active, not recruiting |
Enrollment | 197 |
Est. completion date | December 15, 2022 |
Est. primary completion date | June 15, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years to 75 Years |
Eligibility | Inclusion Criteria: - Participants aged 19 to 75 years with chronic pain. - chronic pain is defined as having non-malignant chronic or persistent pain for at least 6 months. - Participants must experience pain at least half the days in the last 6 months. - Pain can include bodily pain or head (migraine) pain. Exclusion Criteria: - Individuals reporting a cognitive impairment that can interfere with completing questionnaires and using a mobile application. - Individuals reporting any of the following psychiatric illness: schizophrenia, dissociative or personality disorders, bipolar disorder. - Individuals reporting any of the following medical conditions: metastatic cancer, rheumatoid arthritis, lupus, scleroderma, polymyositis. - Individuals reporting substance use disorder (within the last 6 months). - Individuals that have previously used mind-body apps for the treatment of chronic pain. |
Country | Name | City | State |
---|---|---|---|
Canada | University of the Fraser Valley | Chilliwack | British Columbia |
Lead Sponsor | Collaborator |
---|---|
University of the Fraser Valley |
Canada,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Brief Pain Inventory-short form (BPI-SF) | Measures self reported pain intensity (on average); Pain interference | 6 weeks | |
Secondary | Change in PROMIS Pain Intensity short form | Measures self reported pain intensity over 7 days | 6 weeks | |
Secondary | Change in PROMIS Pain Interference short form 8a | Measures self reported pain interference in daily activities (over 7 days) | 6 and 12 weeks | |
Secondary | Change in Pain Catastrophizing Questionnaire (PCS) | Measures thoughts and perceptions of pain | 6 and 12 weeks | |
Secondary | Change in DASS-21 (Depression, Anxiety, and Stress Scale) | Measures self reported emotional states | 6 and 12 weeks | |
Secondary | Change in Quality of Life Short Form 12 (SF-12) | Measures self-reported impact of health on daily life | 6 and 12 weeks | |
Secondary | Change in Brief Pain Inventory-short form (BPI-SF) | Measures self reported pain intensity; Pain interference (over past 24 hours) | 12 weeks | |
Secondary | Change in PROMIS Pain Intensity short form | Measures self reported pain intensity over 7 days | 12 weeks | |
Secondary | Medication use (daily) | Self-reported quantify of medication used (dosage, number of pills in 24 hours) | 6 weeks | |
Secondary | Medication use (occasional) | Self-reported quantify of medication used (dosage, number of pills in 7 days) | 6 weeks |
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