A Pilot Implementation Study of GLA:D Back

Completed

• Conditions: Low Back Pain

• Registration Number: NCT03864224
• Lead Sponsor: University of Alberta

Brief Summary

GLA:D Back is a program developed in Denmark to help people with persistent low back pain. This pilot study will assist in contextualizing Danish content into an English version of the program.

Detailed Description

GLA:D Back is a program developed in Denmark to help people with persistent low back pain. Unfortunately, all materials developed for the program are in Danish. In this pilot, the investigators will translate the Danish materials into English, then use them to conduct an English training session for community clinicians in Edmonton, Alberta, Canada. Interested clinicians will then implement the program in their communities and provide feedback to contextualize the program for use in English. Specifically, surveys, interviews and focus groups will be used to help fine-tune the printed content of the course (e.g. manuals), it's training materials (e.g. lectures) and processes related to REDCap data collection (e.g. surveys).

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2019-02-11
• Study First Submitted: 2019-03-04
• Study First Submitted QC: 2019-03-04
• Study First Posted: 2019-03-06
• Primary Completion: 2020-02-11
• Status Verified: 2022-04
• Study Completion: 2022-06-08
• Last Update Submitted: 2022-07-06
• Last Update Posted: 2022-07-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 190

Inclusion Criteria

• Patients must have persistent low back pain of at least 1 month's duration.

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Exclusion Criteria

• Participating currently in a supervised exercise or rehabilitation program or enrolled in another interventional clinical trial.
• Patients with nerve root involvement, suspected serious pathology, unstable trauma to the spine, aspects of pregnancy or other conditions that would prevent participation or disallow trial completion within the prescribed time period.
• Persons with conditions that require a specialist consult are suspected of needing a specialist consult, or have conditions that would be aggravated or worsened if treated by the interventions in this study.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Implementation	6 months	Number of clinicians who implement the program

Secondary Outcome Measures

Name	Time	Method
Patients enrolled	6 months	Number of patients trained by each GLA:D clinician

Trial Locations

Locations (1)

University of Alberta; 🇨🇦 Edmonton, Alberta, Canada