Peer Partners to Improve Physical Activity in Older Latino and Latina Adults With Parkinson's Disease.
Public ClinicalTrials.gov record NCT06170866. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The goal of this interventional study is to culturally adapt and determine feasibility of the peer partner training program and the peer-supported mobile health physical activity intervention in older Latin/Hispanic people with Parkinson's disease. The main question\[s\] it aims to answer are: * What is the feasibility of the peer partner training program? * What is the feasibility of the peer-supported mobile health physical activity intervention? * What are the effects of the peer-supported mobile health physical activity intervention on physical activity, motivation, depression, apathy and self-efficacy? Participants will be asked to: * Wear a research-grade activity monitor, Actigraph GT9X device for 10 days at the beginning and end of the study. * Watch 11 educational videos about Parkinson´s disease and exercise and attend two virtual educational sessions. * Connect with another person with Parkinson´s disease one time a week on a virtual meeting platform for 8 weeks. * Use Fitbit activity monitors and connect with other participants through the Fitbit application for 8 weeks. * Attend a weekly online exercise class for 8 weeks with other people with Parkinon´s disease.
Study identification
- NCT ID
- NCT06170866
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 10 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 50 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- May 31, 2023
- Primary completion
- Jun 30, 2024
- Completion
- Aug 29, 2024
- Last update posted
- Nov 25, 2025
2023 – 2024
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Connecticut | Storrs | Connecticut | 06269 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06170866, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 25, 2025 · Synced Sep 16, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06170866 live on ClinicalTrials.gov.