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Clinical Trials/NCT06170866
NCT06170866
Completed
N/A

Peer Partners to Improve Physical Activity in Older Latino and Latina Adults With Parkinson's Disease.

UConn Health1 site in 1 country10 target enrollmentJune 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
UConn Health
Enrollment
10
Locations
1
Primary Endpoint
Acceptability of Intervention Measure (AIM)
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

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.
Registry
clinicaltrials.gov
Start Date
June 1, 2023
End Date
August 30, 2024
Last Updated
5 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
UConn Health
Responsible Party
Principal Investigator
Principal Investigator

Cristina Colón-Semenza

Principal Investigator

UConn Health

Eligibility Criteria

Inclusion Criteria

  • Idiopathic Parkinson disease,
  • Able to walk without the assistance of another person for 10 minutes
  • ≥ 29 on Telephone Interview for Cognitive Status (TICS)
  • To have a close friend/family member over the age of 18 that would support the participant during the intervention
  • ≥ 50 years of age
  • To be willing to use an activity monitor and use a Fitbit and Fitbit application
  • To be on a stable course of PD medications without any plans for change over the next 3 months
  • To be able to speak, read and write in Spanish or English

Exclusion Criteria

  • Unstable cardiopulmonary, orthopedic, psychological or metabolic condition
  • Atypical Parkinsonism Disorders
  • A fall in the last 6 months (that was unrelated to an external force)
  • Currently engaging in 150 minutes of mod-vigorous physical activity/week

Outcomes

Primary Outcomes

Acceptability of Intervention Measure (AIM)

Time Frame: After completion of the entire intervention (11 weeks)

A standardized measure of acceptability that indicates percent agreement with acceptability of the intervention ranging from 20-100%. Higher scores indicate agreement (better outcome) with the acceptability of the intervention.

Intervention Appropriateness Measure (IAM)

Time Frame: After completion of the entire intervention (11 weeks)

A standardized measure of appropriateness that indicates percent agreement with appropriateness of the intervention ranging from 20-100%. Higher scores indicate more agreement (better outcome) with the appropriateness of the intervention.

Feasibility of Intervention Measure (FIM)

Time Frame: After completion of the entire intervention (11 weeks)

A standardized measure of feasibility that indicates percent agreement with feasibility of the intervention ranging from 20-100%. Higher scores indicate more agreement (better outcome) with the feasibility of the intervention.

Secondary Outcomes

  • Objective Measurement of Physical Activity(10 days at baseline and post-intervention (approximately 12 to 14 weeks))
  • Behavioral Regulation in Exercise Questionnaire-2 (BREQ-2)(Baseline and post Intervention (approximately 12 to 14 weeks))
  • Parkinson's Disease Questionnaire-39 (PDQ-39)(Pre and post intervention (approximately 12 to 14 weeks))
  • Geriatric Depression Scale-Short Form(Pre and post intervention (approximately 12 to 14 weeks))

Study Sites (1)

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