N/A
N=360
Get Ready And Empowered About Treatment
HIV
Bottom Line
View on ClinicalTrials.gov: NCT02165735 ↗Enrolled (actual)
360
Serious AEs
0.0%
Results posted
Oct 2018
Primary outcome: Primary: Change in Patient Activation Measure (PAM) — 73.35; 70.53 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- patient activation training (Behavioral); Usual care (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Rochester
- Primary completion
- Nov 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Patient Activation Measure (PAM) |
73.35; 70.53 | — |
| SECONDARY Change in eHealth Literacy Scale (eHEALS) |
29.81; 27.67 | — |
| SECONDARY Change in Decisional Self-Efficacy Scale (DSES) |
91.89; 90.81 | — |
| SECONDARY Change in Perceived Involvement in Care Scale (PICS) |
33.74; 32.47 | — |
| SECONDARY Change in Instrument on Doctor Patient Communication Skills (IDPCS) |
85.06; 83.49 | — |
| SECONDARY Change in HIV Adherence Self-Efficacy Scale (ASES) |
102.80; 103.13 | — |
| SECONDARY Change in Self-Reported Adherence |
89.33; 89.90 | — |
| SECONDARY Change in Undetectable Viral Load |
87; 86 | — |
| SECONDARY Change in Evidence-based Preventative Care |
0.35; 0.35 | — |
| SECONDARY Change in Short Form Health Survey: [Mental Health] (SF12) |
46.38; 46.99 | — |
| SECONDARY Change in Short Form Health Survey: [Physical Health] (SF12) |
44.83; 45.13 | — |
Summary
The purpose of this study is to rigorously assess a program designed to empower patient living with HIV, to improve their health care and health, and to reduce disparities.
Eligibility Criteria
Inclusion Criteria
- age18 years or older,
- confirmed HIV diagnosis
- receipt of care within a participating site.
Exclusion Criteria
- inability to provide informed consent
- limited English proficiency (Trainings and Personal Health Record are currently only available in English)
Data sourced from ClinicalTrials.gov (NCT02165735). 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.