MedPath

Preliminary Testing of Cafe Move for Primary Prevention of Physical Frailty

Not Applicable
Recruiting
Conditions
Aging
Registration Number
NCT05720507
Lead Sponsor
University of Montana
Brief Summary

This project explores a novel means of health promotion and prevention of age-related physical frailty, which is designed to overcome barriers to access and promote autonomy in managing physical health.

Detailed Description

The purpose of this investigation is to field-test a physical function assessment paradigm, designed to inform people of their physical function relative to peers of similar demographic characteristics (e.g., similar age, sex, height, etc.), to promote recommended preventive health behaviors. The physical function assessment paradigm is known as Cafe Move. Our primary research hypothesis is that people will advance along the stages of behavior change (i.e., more likely to participate in recommended preventive healthcare for physical function), after accessing Cafe Move assessments. This study is a single cohort (n=36 participants), double-baseline design, intended primarily to collect pilot data. The results will inform the design of a larger controlled trial.

This study will examine the safety, feasibility, acceptability, and preliminary efficacy of Café Move. Briefly, we will make Café Move available to at-risk populations (i.e., independent-living older adults) via the following approach. First, during a 3-month control phase, we will monitor participants' health behaviors and engagement with preventive health offerings via periodic phone surveys. We will then make Café Move available and subsequently monitor health behaviors and engagement with preventive health offerings. This design will allow us to examine feasibility of the Café Move intervention, to better understand the reach of the program within and across communities, and to determine variance and covariance for the outcome measures of interest.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
36
Inclusion Criteria
  • Legally autonomous to consent
  • Lives independently
  • Ability to sit, stand, and walk without the assistance of another person
Exclusion Criteria
  • Not legally autonomous to consent
  • Institutionalized

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Health Behavior Stages of Change Questionnairethrough study completion, average of 4-6 months

Self-reported measure of engagement with preventive care or wellness activities

Secondary Outcome Measures
NameTimeMethod
Healthcare Access and Utilization Questionnairethrough study completion, average of 4-6 months

Self-reported measure of healthcare utilization of a number of different services

Trial Locations

Locations (1)

University of Montana

🇺🇸

Missoula, Montana, United States

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