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mPATH for Low-income Older Adults

mHealth-Facilitated Physical Activity Toward Health (mPATH) Intervention for Low-Income Older Adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05935241
Enrollment
176
Registered
2023-07-07
Start date
2024-05-30
Completion date
2029-12-31
Last updated
2026-04-13

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

Conditions

Cognitive Decline, Insomnia, Sedentary Time

Keywords

physical activity, memory, sleep

Brief summary

Although empirical research suggests that physical activity interventions benefit cognition and sleep in older adults in general, the possible benefit of physical activity is understudied in low-income older adults. The study aims to test the immediate and sustaining efficacy of an mHealth-facilitated Physical Activity Toward Health (mPATH) intervention on cognitive function and sleep in low-income older adults.

Detailed description

Low-income older adults (LIOA) are a population at higher risk to develop Alzheimer's disease and related dementias (ADRD) and sleep disturbances. Although empirical research suggests that physical activity interventions benefit cognition and sleep in older adults in general, the possible benefit of physical activity is understudied in LIOA. The growing wearable device and mobile Health (mHealth) provide an innovative approach to deliver individually tailored physical activity interventions at home with flexible schedules to overcome barriers to physical activity in LIOA. In addition, limited research has examined if physical activity interventions impact the individual's Amyloid/Tau/ Neurodegeneration (ATN) Alzheimer's disease biological state and whether physical activity may promote cognition through impacting sleep and AD pathology. This randomized controlled trial is designed to examine the immediate and sustaining efficacy of an mHealth-facilitated Physical Activity Toward Health (mPATH) intervention on cognitive function and sleep in LIOA. mPATH is a personalized physical activity intervention that includes personalized physical activity plans and training sessions, exercise at home by following personalized exercise videos, and biweekly phone coaching over 24 weeks, supported by wearable devices-enabled mHealth strategies. mHealth strategies and exercise videos will be used to support participant's physical activity during 6-12months.

Interventions

BEHAVIORALmPATH

The active mPATH intervention takes 6 months including (1) The physical activity education session , (2)mHealth learning and practice; (3)Personalized physical activity training, plan, and biweekly phone calls over 24 weeks (4) mHealth strategies to encourage physical activity and facilitate intervention adherence (5) (5) mPATH during 6-12 months: mPATH will be delivered mainly in 24 weeks before the 6-month data collection. During 6-12 months, the participants will have access to study mHealth strategies, and exercise videos. No additional physical activity training by staff will be supported.

OTHERAttention Control

A registered nurse from the study team will provide 6 monthly home visit (approximately 55-60 minutes each) to provide physical activity education, physical activity safety at home evaluation, feedback, and social activity (meaningful or enjoyable activities as identified by the participants, such as playing cards, doing arts and crafts, listening to music, talking about life history, etc.).

Sponsors

Johns Hopkins University
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* self-reported difficulty of sleep * lack of physical activity/exercise * low household income * capacity for moderate intensity exercise

Exclusion criteria

* untreated sleep apnea * severe depression or anxiety * dementia * history of neurologic or psychiatric disorders, neurodevelopmental impairment, traumatic brain injury * current enrollment in another clinical trial

Design outcomes

Primary

MeasureTime frameDescription
Change in episodic memory as assessed by the CogstateBaseline, 6 months, 12 monthsEpisodic memory will be measured by computerized cognitive batteries using Cogstate

Secondary

MeasureTime frameDescription
Change in Sleep efficiency as assessed by actigraphyBaseline, 6 months, 12 monthssleep efficiency will be measured by 7-day actigraph (reported as a percentage)

Countries

United States

Contacts

CONTACTJunxin Li
junxin.li@jhu.edu4105022608
CONTACTJulianna Kruemmel
jkruemm1@jh.edu443-692-7169
PRINCIPAL_INVESTIGATORJunxin Li

Johns Hopkins University

STUDY_DIRECTORYoungmin Cho, PhD

Johns Hopkins University School of Nursing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026