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N/A Completed N=36 Randomized Single-blind Treatment

Improving Quality of Life for Adults Living With HIV and Chronic Pain

Source: ClinicalTrials.gov NCT05055596 ↗
Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcomePrimary: Pain Intensity - Brief Pain Inventory — 7.3; 6.6; 6.1; 6.1 units on a scale

Summary

Chronic pain is highly comorbid among the 1.2 million persons living with HIV, with recent prevalence estimates ranging from 55-67%. Needed are evidenced-based non-pharmacological interventions to improve chronic pain management and reduce the demand for opioids in the United States. The proposed research will address this need by examining the feasibility and acceptability of Tai Chi as a mind-body intervention for chronic pain management in an HIV population.

Outcome Measures

OutcomeResultp-value
PRIMARY
Pain Intensity - Brief Pain Inventory
7.3; 6.6; 6.1; 6.1; 5.6; 7.4
PRIMARY
Pain Interference - Brief Pain Inventory
5.9; 5.8; 4.7; 5.8; 5.4; 6.5
PRIMARY
Feasibility to Execute Study Protocol
16; 16; 2; 2; 16; 16
PRIMARY
Participant Satisfaction Questionnaire (PSQ) - Acceptability
11; 10; 3; 4; 2; 2
SECONDARY
Perceived Stress Scale (PSS)
25.7; 28.1; 26.0; 26.6; 26.9; 26.3
SECONDARY
Patient Health Questionnaire (PHQ-8)
10.8; 12.4; 9.4; 10.3; 9.1; 9.4

Eligibility Criteria

Inclusion Criteria

  • age 45 and older;
  • HIV positive status based on clinical records;
  • chronic pain condition based on clinical records;
  • English speaking;
  • physically able to participate in a Tai Chi program

Exclusion Criteria

  • Inability or unwillingness to provide informed consent
  • Inability or unwillingness to travel to Temple Dental School;
  • Inability or unwillingness to engage in 10-week intervention;
  • Non-English speaking;
  • Active substance use disorder;
  • Acutely suicidal or psychotic;
  • Self-reported participation in another research study related to chronic-pain
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05055596). 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.

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