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.
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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)