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NCT04102514 · ClinicalTrials.gov registry record · NA

A Dyadic Approach for a Remote Physical Activity Intervention in Adults With AD and Their Caregivers

A NA study of Alzheimer Disease, sponsored by University of Kansas.

Completed
Registry status
NA
Development phase
198
Enrollment target
1
Study location

NCT04102514: Completed NA study of Alzheimer Disease, sponsored by University of Kansas.

NCT04102514 is a NA study of Alzheimer Disease that has completed, run by University of Kansas. The registered enrollment target is 198 participants, below the 2,750-participant average among 306 other Alzheimer Disease trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04102514, a NA study of Alzheimer Disease, has completed, sponsored by University of Kansas.

COMPLETED
Registry status
NA
Development phase
198 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to compare the effectiveness of 2 intervention delivery strategies for increasing moderate physical activity (MPA), real-time group video conferencing (RGV) vs. enhanced usual care (EUC), in community dwelling adults with Alzheimer's diseases (AD) and their caregiver (dyads) over 18 mos. (6 mos. active, 6 mos. maintenance, 6 mos. no contact). The primary outcome is to compare total MPA (min/wk.), assessed using ActiGraph, in adults with AD from baseline to 6 mos. Secondary aims for the Adults with AD are to compare MPA (min/wk), sedentary time (min/wk.), percentage meeting 150 min/wk. goal, functional fitness, activities of daily living (basic/instrumental), quality of life, residential transitions, and cognitive function across 18 months between RGV and EUC. Secondary aims for the caregivers are to compare total MPA (min/wk.), sedentary time (min/wk.), functional fitness, quality of life, caregiver burden across 18 months between RGV and EUC. Additionally, as an exploratory aim, this study will evaluate the influence of process variables/participant characteristics on MPA in adults with AD and their caregiver across 6, 12 \& 18 mos.: age, sex, BMI, attendance (exercise/support sessions), use of recorded videos, PA self-monitoring, peer interactions during group sessions, caregiver support, type and quality of dyadic relationship, and number of caregivers.

Primary Outcome

Moderate physical activity will be assessed using an ActiGraph model wGT3x-BT triaxial at baseline, 3, 6, 12 and 18 months. The ActiGraph wGT3x-BT is worn on a belt on the non-dominant hip during all waking hours for one week (7 consecutive days), with the exception of bathing, and swimming. The device measures acceleration. The acceleration values are used to determine levels of physical activity using previously validated cutpoints. Data were considered valid if they wore the accelerometer for

Conditions Studied

Interventions

  • BEHAVIORAL Enhanced Usual Care
  • BEHAVIORAL Real-time Group Video

Study Locations (1)

Kansas

  • University of Kansas - Lawrence

Trial Details

FieldValue
Enrollment Target 198 participants
Start Date 2020-07-06
Est. Completion 2024-08-19
Phase NA
University of Kansas

66 total trials

What the finished NCT04102514 record still lists

NCT04102514 is an interventional study that assigns participants to a tested intervention. The registered 198 participants enrollment target is mid-sized for trials with a published cap, below the 2,750-participant average among 306 other Alzheimer Disease trials with a reported enrollment target (93% lower).

The record links to 1 condition, with Alzheimer Disease appearing as the primary indexed condition, and to 2 interventions - of which Enhanced Usual Care is the first listed.

NCT04102514 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT04102514 about?

NCT04102514 is a clinical study titled "A Dyadic Approach for a Remote Physical Activity Intervention in Adults With AD and Their Caregivers". The objective of this study is to compare the effectiveness of 2 intervention delivery strategies for increasing moderate physical activity (MPA), real-time group video conferencing (RGV) vs. enhanced usual care (EUC), in community dwelling adults with Alzheimer's diseases (AD) and their caregiver (...

What is the current status of trial NCT04102514?

This trial is currently completed. It is a NA study. The enrollment target is 198 participants. The study started on 2020-07-06. Estimated completion is 2024-08-19.

What conditions does trial NCT04102514 study?

This clinical trial studies the following conditions: Alzheimer Disease.

What interventions are being tested in trial NCT04102514?

The interventions under investigation include: Enhanced Usual Care (BEHAVIORAL), Real-time Group Video (BEHAVIORAL).

Who is sponsoring clinical trial NCT04102514?

This trial is sponsored by University of Kansas, which has 66 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04102514 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Alzheimer Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04102514's enrollment target sits among peer trials

198 112th of 306 higher than 195 of 306 other Alzheimer Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Alzheimer Disease 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 NCT04102514, the US trial registry maintained by the National Library of Medicine. NCT04102514 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.