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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05090683
Other study ID # 100820
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 15, 2021
Est. completion date December 15, 2022

Study information

Verified date November 2022
Source University of the Fraser Valley
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mind-body mobile application
Self-directed; Study team will recommend daily use of mobile app for 6 weeks with a minimum of 4 times/week usage of mobile app for 6 weeks. Frequency will be monitored via weekly surveys.

Locations

Country Name City State
Canada University of the Fraser Valley Chilliwack British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of the Fraser Valley

Country where clinical trial is conducted

Canada, 

References & Publications (13)

Ashar YK, Gordon A, Schubiner H, Uipi C, Knight K, Anderson Z, Carlisle J, Polisky L, Geuter S, Flood TF, Kragel PA, Dimidjian S, Lumley MA, Wager TD. Effect of Pain Reprocessing Therapy vs Placebo and Usual Care for Patients With Chronic Back Pain: A Randomized Clinical Trial. JAMA Psychiatry. 2022 Jan 1;79(1):13-23. doi: 10.1001/jamapsychiatry.2021.2669. — View Citation

Borm GF, Fransen J, Lemmens WA. A simple sample size formula for analysis of covariance in randomized clinical trials. J Clin Epidemiol. 2007 Dec;60(12):1234-8. Epub 2007 Jun 6. — View Citation

Cleeland CS, Ryan KM. Pain assessment: global use of the Brief Pain Inventory. Ann Acad Med Singap. 1994 Mar;23(2):129-38. Review. — View Citation

Gatchel RJ, Peng YB, Peters ML, Fuchs PN, Turk DC. The biopsychosocial approach to chronic pain: scientific advances and future directions. Psychol Bull. 2007 Jul;133(4):581-624. Review. — View Citation

GBD 2016 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2017 Sep 16;390(10100):1211-1259. doi: 10.1016/S0140-6736(17)32154-2. Erratum in: Lancet. 2017 Oct 28;390(10106):e38. — View Citation

Kean J, Monahan PO, Kroenke K, Wu J, Yu Z, Stump TE, Krebs EE. Comparative Responsiveness of the PROMIS Pain Interference Short Forms, Brief Pain Inventory, PEG, and SF-36 Bodily Pain Subscale. Med Care. 2016 Apr;54(4):414-21. doi: 10.1097/MLR.0000000000000497. — View Citation

Lovibond PF, Lovibond SH. The structure of negative emotional states: comparison of the Depression Anxiety Stress Scales (DASS) with the Beck Depression and Anxiety Inventories. Behav Res Ther. 1995 Mar;33(3):335-43. — View Citation

Morone NE, Greco CM. Mind-body interventions for chronic pain in older adults: a structured review. Pain Med. 2007 May-Jun;8(4):359-75. Review. — View Citation

Osman A, Barrios FX, Kopper BA, Hauptmann W, Jones J, O'Neill E. Factor structure, reliability, and validity of the Pain Catastrophizing Scale. J Behav Med. 1997 Dec;20(6):589-605. — View Citation

Pfeifer AC, Uddin R, Schröder-Pfeifer P, Holl F, Swoboda W, Schiltenwolf M. Mobile Application-Based Interventions for Chronic Pain Patients: A Systematic Review and Meta-Analysis of Effectiveness. J Clin Med. 2020 Nov 5;9(11). pii: E3557. doi: 10.3390/jcm9113557. Review. — View Citation

Schopflocher D, Taenzer P, Jovey R. The prevalence of chronic pain in Canada. Pain Res Manag. 2011 Nov-Dec;16(6):445-50. — View Citation

Treede RD, Rief W, Barke A, Aziz Q, Bennett MI, Benoliel R, Cohen M, Evers S, Finnerup NB, First MB, Giamberardino MA, Kaasa S, Kosek E, Lavand'homme P, Nicholas M, Perrot S, Scholz J, Schug S, Smith BH, Svensson P, Vlaeyen JWS, Wang SJ. A classification of chronic pain for ICD-11. Pain. 2015 Jun;156(6):1003-1007. doi: 10.1097/j.pain.0000000000000160. — View Citation

Ware J Jr, Kosinski M, Keller SD. A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996 Mar;34(3):220-33. — View Citation

* Note: There are 13 references in allClick here to view all references

Outcome

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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