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Exercise Adherence and Cognitive Decline

Exercise Adherence and Cognitive Decline: Engaging With the Black Community to Develop and Test a Goal-Setting and Exercise Intensity Intervention

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06769022
Acronym
MOVE
Enrollment
21
Registered
2025-01-10
Start date
2024-10-01
Completion date
2025-07-07
Last updated
2026-06-11

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

Conditions

Cognitive Decline

Keywords

Goals, Exercise Intensity, Goal Difficulty, Cognitive Decline

Brief summary

The purpose of this study is to conduct a small-scale test of a goals-based program to help people to exercise more and learn what people like or don't like about the procedures. This program is being designed for individuals aged 45-65 from the Black community. Low levels of physical activity are related to health problems such as heart disease, diabetes, and cognitive decline. People of color are more negatively impacted by these conditions and have also historically been underrepresented by research seeking to increase physical activity. The investigators have developed this goals-based exercise promotion program with the help of a Black-led community-based organization (The Gyedi Project) and a Community Advisory Board made up of stakeholders in the Black community, and now the investigators are conducting a trial of its feasibility and acceptability.

Interventions

Participants' goal-setting and exercise intensity are manipulated based on group assignment.

Sponsors

University of Colorado, Boulder
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* \<3 incorrect responses on the Pfeiffer Mental Status Questionnaire * Ages 45-65. * Consent to be randomized to condition. * Planning to remain in the Denver metro area for the next two months * Identify as Black or African American

Exclusion criteria

* Currently physically active (i.e., \>90 min/week of moderate PA or \>40 min/week of vigorous PA consistently for the past 6 months). * On antipsychotic medications or currently under treatment for any serious psychiatric disorder, including Alzheimer's or dementia * Answers "yes" to 1 or more of the 7 questions of the PAR-Q+ * Blood pressure at baseline or before exercise is greater than 140/90 * Blood pressure \>210/90 mmHg (for men) or \>190/90 mmHg (for women) immediately after exercise * Inability to walk 3 blocks without chest pain, shortness of breath, or light headedness. * Inability to climb 2 flights of stairs without chest pain, shortness of breath, or light headedness.

Design outcomes

Primary

MeasureTime frameDescription
Blood PressureBaseline, Visit 14 (~2 months after baseline)Blood pressure of all participants is collected before intervention
Activity LevelsBaseline, Visit 14 (~2 months after baseline)Exercise Intensity (PAR). Answers are direct (ex. how many hours active) and not scaled. Information is requested for the week and the past 3 months.
Sleep levelsBaseline, Visit 14 (~2 months after baseline)Exercise Intensity (PAR). Answers are direct (ex. how many hours did you sleep) and are not scaled. Information is requested for the past 7 days.
Physical Activity RecallBaseline, Visit 14 (~2 months after baseline)Exercise Intensity (PAR). Answers are direct (ex. how many hours did you sleep) and are not scaled. Information is requested for the past 7 days.
IdentityBaselineMultidimensional Black Identity Scale to collect information on identity. Questions are about personal identity relating to the Black community on a scale of 1-7, 1 being strongly disagree and 7 being strongly agree. Higher scores indicate a stronger agreement with that dimension of Black identity. Scores are summed as subscales and averaged to obtain an average score.
Exercise BehaviorBaseline, Visit 14 (~2 months after baseline)CHAMPS. The survey collects quantitative data looking at the approximate total hours per week spent doing various activities, both physical and social.
Theoretical Mediators of Exercise BehaviorBaseline, Visit 12 (~1 month after baseline), Visit 14 (~2 months after baseline)Intrinsic Motivation Inventory. Questions relate to how participants think or feel about physical activity, with answers ranging from 1 (strongly disagree) to 7 (strongly agree). Broader scores are broken up into subscales; final subscale scores are summed and averaged. Higher scores indicate higher agreement with that subscale.
Heart Rate VariabilityBaseline, Visit 14 (~2 months after baseline)Heart Rate Variability is measured using chest strap monitor.
Heart RateBaseline, Visits 1-14 (all visits)HR is measured using chest strap monitor.
Physical PerformanceBaseline, Visit 14 (~2 months after baseline)Short Physical Performance Battery. Physical performance measured with repeated chair stands, three balance tests (side-by-side, semi-tandem, tandem), timed walking.
Ventilatory ThresholdBaselineTalk Test. Graded treadmill test where intensity is increased at intervals to determine participant's ventilatory threshold.
Perceived ExertionVisit 2-13 (~2 visits/week)A single-item measure from Borg (1973) was used to assess participants' rate of perceived exertion (RPE) during the exercise bout. Participants were asked to rate the average intensity of exercise \[at that moment/during the past ten minutes\] on a 25-point scale ranging from 6 (no exertion at all) to 20 (maximal exertion).
Pain LevelsVisit 2-13 (~2 visits/week)A single item measure from Borg (1998) was used to assess participants' pain levels during the exercise bout. Participants were asked to indicate how much pain they felt \[at that moment/during the past ten minutes\] on an 11-point scale ranging from 0 (nothing at all) to 10 (excruciating).
Affective ValenceVisit 2-13 (~2 visits/week)The Feeling Scale, a single-item measure from Hardy and Rejeski (1989), was used to assess participants' affective valence during the exercise bout. Participants were asked to indicate how they felt \[at that moment/during the past ten minutes\] on an 11-point scale ranging from -5 (very bad) to +5 (very good).
Affective ArousalVisit 2-13 (~2 visits/week)The Felt Arousal Scale, a single-item measure from Svebak and Murgatroyd (1985), was used to assess participants' affective arousal during the exercise bout. Participants were asked to indicate how "worked-up" they felt \[at that moment/during the past ten minutes\] on a 6-point scale ranging from 1 (low arousal) to 6 (high arousal).
EnjoymentVisit 2-13 (~2 visits/week)A single item measure from Gillman and Bryan (2015) was used to assess participants' enjoyment levels during the exercise bout. Participants were asked to indicate how enjoyable exercise was \[at that moment/during the past ten minutes\] on a 5-point scale ranging from 1 (no enjoyment at all) to 5 (a great deal of enjoyment).
Exercise Check-InDaily between visit 13 and 14 (~1 month)Three short questions assessing if the participant planned to engage in exercise and how many minutes of moderate (0-120) and vigorous (0-60) exercise they engaged in
Study FeedbackVisit 14 (~2 months after baseline)An investigator led interview to pilot study participants' experience of the intervention and suggestions for improvement
Exercise Benefits and BarriersBaseline, Visit 12 (~1 month after baseline), Visit 14 (~2 months after baseline)A 10 item scale assessing perceived benefits of and barriers to exercise
AnthropometricsBaselineHeight, weight, waist circumference, and hip circumference will be measured
Exercise Aligned with Black IdentityBaselineAssessment of the extent to which 7 common exercises are aligned with Black identity
Mental StatusBaselinePfeiffer Mental Status. Assessment of cognitive deficits at baseline.
DietBaselineNutrition Data System for Research (NDSR) 24-Hour Dietary Recall. Interviewer administered recall developed by the University of Minnesota Nutrition Coordinating Center (NCC).
Physical ActivityBaselineGodin Survey. This survey measures time spent in moderate, strenuous or light activity and has been modified to include time spent sitting over a typical 7 day period. Scores are summed and a range is used to quantify how active/sedentary a participant is.

Secondary

MeasureTime frameDescription
DemographicsBaselineSurvey includes sex assigned at birth, gender identity, sexual orientation, age, detailed race/ethnicity, and SES

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026