The Web-Based Pain-at-Work Toolkit With Telephone Support for Employees With Chronic or Persistent Pain: Protocol for a Cluster Randomized Feasibility Trial
JMIR Research Protocols · 11 authors, 9 centres
AI SUMMARY
FIDELITY 100%
This summary was generated by AI from a single paper. It has not been reviewed by a clinician and is not clinical advice. Verify against the source before acting on it.
The primary aim is to establish feasibility parameters like recruitment and acceptability, not to test the intervention's effectiveness.
Full summary
823 CHARS
The primary objective is to assess the feasibility of conducting a definitive trial by measuring recruitment, retention, intervention fidelity, and acceptability. Secondary aims include exploring employer outcomes and participant-reported outcome measures to inform the design of a future trial. The study will recruit 120 participants from at least 8 workplace clusters in England. Randomization occurs at the cluster level, with participants unblinded. A nested qualitative study will explore acceptability. As a feasibility study, it is not designed to test the clinical effectiveness of the intervention. The main limitation noted is the challenge of recruiting and retaining participants in workplace research. Findings will inform the sample size, outcomes selection, and health economic model for a definitive trial.