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Promoting In-Home Activities at a Memory & Aging Clinic

Promoting In-Home Activities at a Memory & Aging Clinic (Pro-Home MeC)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05771064
Acronym
Pro-Home MeC
Enrollment
28
Registered
2023-03-16
Start date
2023-03-21
Completion date
2025-05-05
Last updated
2025-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MCI, Mild Dementia

Brief summary

The objective of the proposed study, Promoting In-Home Activities at a Memory & Aging Clinic (Pro-Home MeC), is to assess and improve the feasibility of a physical activity (PA) intervention and the measurement of cognitive outcomes in a memory clinic setting for inactive older adults with mild cognitive impairment (MCI) or mild dementia and to examine how and improve the feasibility and acceptability of the procedures.

Interventions

BEHAVIORALGentle Moves

A safe physical activity program which consists of a brief motivational enhancement and three movements to be performed in a seated position; and two movements in the standing position. The intervention will be delivered by a research coach.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
University of Illinois at Chicago
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 50+ * Fluent in English * Diagnosed with MCI or mild dementia * Physically inactive (\< 150 min/wk of planned PA) * Able to sit in a chair independently for 15+ minutes

Exclusion criteria

* Have significant mental or physical disabilities that lead to inability to perform PA safely (e.g., major stroke) * Severe uncompensated hearing or visual loss * Having insufficient decisional capacity to consent to participate in research. * Lack of safety awareness * Unwilling to be assigned to Pro-Home MeC or control group * Currently participating in PA intervention research

Design outcomes

Primary

MeasureTime frameDescription
Program Feasibility3 months• Program feasibility measured by program adherence (e.g., self-reported program activities in the past 24 hours, yes/no).
Program Acceptability3 months• Program acceptability measured by patient's perception of the program difficulty. (Too hard, a little too hard, just right, a little too easy, much easy)
Feasibility of NIH Toolbox Cognition Battery3 monthsFeasibility of NIH Toolbox Cognition Battery measured by administration time.

Secondary

MeasureTime frameDescription
NIH Toolbox Cognition Battery scores3 monthsNIH Toolbox Cognition Battery Fluid Cognition scores (range 59 - 140, higher score means better cognition)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026