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NCT07171255 · ClinicalTrials.gov registry record · NA

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

A NA study of Sedentary Middle Age and Older Aged Adults, sponsored by Creighton University.

Recruiting
Registry status
NA
Development phase
54
Enrollment target
2
Study locations

NCT07171255: Recruiting NA study of Sedentary Middle Age and Older Aged Adults, sponsored by Creighton University.

NCT07171255 is a NA study of Sedentary Middle Age and Older Aged Adults that is actively recruiting participants, run by Creighton University. The registered enrollment target is 54 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07171255, a NA study of Sedentary Middle Age and Older Aged Adults, is actively recruiting participants, sponsored by Creighton University.

RECRUITING
Registry status
NA
Development phase
54 participants
Enrollment target
2
Study locations

Study 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 res

Interventions

  • BEHAVIORAL RemoteEx+ Programming

Study Locations (2)

Kansas

  • Emporia State University - Emporia

Nebraska

  • Creighton University - Omaha

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2025-08-22
Est. Completion 2026-06-30
Phase NA
Creighton University

98 total trials

What NCT07171255 shows while recruiting

NCT07171255 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Sedentary Middle Age and Older Aged Adults appearing as the primary indexed condition, and to 1 intervention - of which RemoteEx+ Programming is the first listed.

NCT07171255 reports a single indexed study location in Kansas, Nebraska.

Frequently Asked Questions

What is clinical trial NCT07171255 about?

NCT07171255 is a clinical study titled "Improving Exercise Adherence With App Technology for At-Risk Adults Living in Rural Kansas and Nebraska". 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 pro...

What is the current status of trial NCT07171255?

This trial is currently recruiting. It is a NA study. The enrollment target is 54 participants. The study started on 2025-08-22. Estimated completion is 2026-06-30.

What conditions does trial NCT07171255 study?

This clinical trial studies the following conditions: Sedentary Middle Age and Older Aged Adults.

What interventions are being tested in trial NCT07171255?

The interventions under investigation include: RemoteEx+ Programming (BEHAVIORAL).

Who is sponsoring clinical trial NCT07171255?

This trial is sponsored by Creighton University, which has 98 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07171255 being conducted?

This trial has 2 study locations across Kansas, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT07171255's enrollment target sits among peer trials

54 1269th of 2000 higher than 730 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07171255, the US trial registry maintained by the National Library of Medicine. NCT07171255 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.