N/A
Completed N=16
Community-Engaged Options to Facilitate Opioid Reduction
Source: ClinicalTrials.gov NCT05098158 ↗Enrolled (actual)
16
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcomePrimary: Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity Rating — 68.3; 64.4 score on a scale — p=<0.001
Summary
This study investigates how adults prescribed opioids for chronic noncancer pain respond to invitations to try non-opioid options of massage therapy, yoga therapy, chiropractic and physical therapies. Options will be available via telehealth consultation visits using a computer or smartphone with internet connection. The investigators will measure effects on pain, pain-related symptoms, and opioid use over time using a single-group design.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity Rating |
68.3; 64.4 | <0.001 sig |
| PRIMARY PROMIS Pain Interference Rating |
69.9; 64.3 | 0.003 sig |
| SECONDARY Depressive Symptoms Using Patient Health Questionnaire (PHQ-8) |
10.7; 7.6 | 0.011 sig |
| SECONDARY PROMIS Self-efficacy for Managing Symptoms Short Form 4a |
39.4; 41.2 | 0.168 |
| SECONDARY PROMIS Self-efficacy for Managing Emotions Short Form 4a |
43.4; 44.4 | 0.456 |
| SECONDARY Anxiety Using Generalized Anxiety Disorder (GAD-7) |
5.9; 5.2 | 0.517 |
| SECONDARY Interpersonal Needs Questionnaire |
27.7; 24.5 | 0.012 sig |
| SECONDARY Current Opioid Misuse Measure |
7.1; 6.8 | 0.811 |
| SECONDARY Spiritual Well-being Index |
15; 15.1 | 0.941 |
Eligibility Criteria
Inclusion Criteria
- enrollment in treatment at the CHAS Perry St or partnering clinic;
- age greater than 18 years;
- ability to read, speak, and write English;
- diagnosed with a chronic, non-cancer-based painful medical condition;
- ability to provide informed consent.
Exclusion Criteria
- pregnancy;
- diagnosis of a cancer-based painful medical condition;
- any other medical or psychiatric condition that the PI or Co-PI physician of record determine might compromise safe study participation (including but not limited to active psychosis, history of frequent psychiatric hospitalizations, severe anxiety with claustrophobia, aggression)
Data sourced from ClinicalTrials.gov (NCT05098158). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.