The goal of this study is to conduct a feasibility open pilot study (N=5) of HIPS with virtual exit interviews among adult patients with chronic hip joint-related pain (HRP). We will use this mixed methods information to assess the feasibility, credibility, and acceptability of the HIPS intervention and optimize the program and study methodology in preparation for a pilot feasibility randomized control trial (RCT). Deliverables: \[1\] Adapt and refine open pilot protocol, patient recruitment, provider training, and other study materials. \[2\] Assess the feasibility, acceptability, and credibility of HIPS in preparation for a future feasibility RCT.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Proportion of Participants Who Scored Above the Midpoint on Each Subscale of the Credibility and Expectancy Questionnaire
Timeframe: Baseline (0 Weeks)
Proportion of Participants Who Scored Above the Midpoint on the Client Satisfaction Scale
Timeframe: Post-Test (6 Weeks)
Feasibility of recruitment
Timeframe: Baseline (0 Weeks)
Rate at which program was accepted, measured by number of completed program sessions
Timeframe: Post-Test (6 Weeks)
Feasibility of Assessments at Baseline
Timeframe: Baseline (0 Weeks)
Feasibility of Assessments at Post-Test
Timeframe: Post-Test (6 Weeks)
Feasibility of Assessments at Follow-Up
Timeframe: Follow-Up (30 Weeks)
Adverse Events
Timeframe: Collected during intervention, an average of 6 weeks
Therapist adherence
Timeframe: Collected during intervention, an average of 6 weeks
Proportion of participants who report symptom improvements as measured by the Global Rating of Change Scale
Timeframe: Post-Test (6 Weeks)