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Improving Exercise Adherence With App Technology for At-Risk Adults Living in Rural Kansas and Nebraska

Improving Exercise Adherence With App Technology for At-Risk Adults Living in Rural Kansas and Nebraska

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07171255
Acronym
RemoteEx+
Enrollment
54
Registered
2025-09-12
Start date
2025-08-22
Completion date
2026-06-30
Last updated
2025-09-12

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

Conditions

Sedentary Middle Age and Older Aged Adults

Brief summary

Alzheimer's disease and related dementias are a public health crisis impacting individuals across the world. In the United States, adults living in rural areas face an elevated risk for cognitive impairment mainly due to disparities in care, higher sedentary behavior, and reduced education. This project proposes to assess the impact of a remotely delivered exercise program (i.e., RemoteEx+) through a smartphone application. The app is programmed by our team and provides video demonstrations of exercises, workout regimes, motivational messaging, and weekly ADRD risk reduction education. The project aims to assess with a pre/post design the following aims: * Aim 1. Assess the RemoteEx+ intervention exercise adherence, efficacy, enjoyment, and quality of life. We hypothesize that rural adults will report high exercise adherence (80% of session adherence), efficacy (\>50% on Self Efficacy for Exercise), and enjoyment (\>5.0 on Intrinsic Motivation Inventory - Interest / Enjoyment Subscale) and that these variables will be positively correlated with quality of life scores (36-Item Short Form Health Survey \[SF-36\]) * Aim 2. Determine the impact of a technology-driven exercise program on blood pressure and functional mobility associated with dementia risk. We hypothesize that the exercise program will result in improvements in blood pressure and functional mobility (2-minute step test and 30-second chair rise test) and that participants with high exercise adherence will see the greatest improvements in biomarkers associated with reduced dementia risk. * Aim 3. Reduce health disparities among rural-dwelling Nebraska and Kansas residents. We hypothesize that RemoteEx+ will reduce barriers to exercise (Barriers to Being Active Quiz and improve knowledge surrounding dementia and modifiable risk factors (Dementia Knowledge Assessment Tool - Version 2 \[DKAT2\]) that will result in fewer lifestyle-related health disparities for the communities involved in this study. The results from this project will inform whether RemoteEx+ has an impact on the stated outcomes above for adults living in rural areas.

Interventions

BEHAVIORALRemoteEx+ Programming

The exercise program will include video instruction for all exercises, motivational cues, and ADRD risk education throughout the 16-week exercise program to encourage exercise adherence. RemoteEx+ is optimized to enhance exercise knowledge surrounding dementia risk factors to facilitate ADRD risk reduction and overall health improvement. The purpose of this study is to investigate the efficacy of RemoteEx+ on health outcomes associated with dementia risk in underactive rural adults.

Sponsors

Creighton University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 40-85 years * Characterized as underactive by the Telephone Assessment of Physical Activity (TAPA)50 * Self-reported proficiency in English * Own a smartphone and willing to download an application * Primary care provider clearance to participate for those who do not pass the PAR-Q+51 * Live in a rural area (Rural-Urban Commuting Area \[RUCA\] Codes) 52

Exclusion criteria

* Contraindications to high-intensity exercise * Cognitive impairment (\<19 on the Telephone Montreal Cognitive Assessment \[MoCA\]) * Neurodegenerative or acute neurological diagnoses (e.g., Parkinson's disease, stroke, traumatic brain injury) * Orthopedic surgery or injuries in the last 6 months

Design outcomes

Primary

MeasureTime frame
Systolic Blood PressureBaseline and Week 16

Secondary

MeasureTime frameDescription
Cardiovascular EnduranceBaseline and Week 162-Minute Step Test
Lower Extremity StrengthBaseline and Week 1630-second chair rise test
Exercise AdherenceBaseline and Week 16% of sessions completed over the 16-week program
Exercise EfficacyBaseline and Week 16Self Efficacy for Exercise (SEE) Scale (points)
Quality of Life ImprovementBaseline and Week 1636-Item Short Form Health Survey
Barriers to Being ActiveBaseline and Week 16Barriers to Being Active Quiz
Knowledge of dementiaBaseline and Week 16Dementia Knowledge Assessment Tool

Countries

United States

Contacts

Primary ContactRashelle Hoffman, PT, DPT, PhD
rashellehoffman@creighton.edu402-546-8997
Backup ContactErin Blocker, PhD
eblocker@emporia.edu

Outcome results

None listed

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