Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05002660
Other study ID # R01CA230738
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 3, 2023
Est. completion date June 30, 2026

Study information

Verified date June 2023
Source Texas A&M University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a community randomized controlled trial to evaluate a civic engagement curriculum through which residents will identify barriers and facilitators to healthy eating and physical activity and then implement a project in their communities.


Description:

The purpose of this research is to better understand how resident-led activities to change the community environment affect health. The Change Club is a small group of residents who will try to change their community environment relative to food (for example, foods in restaurants or schools) or physical activity opportunities (for example, parks or walking trails) by following a step-wise process facilitated by an extension educator. The purpose of this research is to better understand if and how these activities affect individual behaviors (for example physical activity) and health outcomes (for example BMI) of adults in rural communities. This study will take place in designated rural communities in Texas and New York. It is planned that about 2,260 people will participate in this study. Some will participate as Change Club members; some will participate as family and friends of Change Club members; and others will participate as community residents.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 2831
Est. completion date June 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: We will be recruiting Change Club members (CCM), friend and family members (FFM) of CCM, and community residents (CR). Common inclusion criteria include: - Age 18-99 - English-speaking CCM also must: - Provide consent electronically - Be willing to be randomized to either group - Score "poor" or "intermediate" on at least one of the Simple 7 composite score items (e.g. not meeting Physical Activity Guidelines for Americans) - Live in one of the designated towns in NY and TX FFM also must: - Provide consent electronically - Be family members or friends identified by a CCM CR also must: - Provide consent electronically - Live in one of the designated towns in NY and TX Exclusion Criteria: - Cognitive impairment (if it precludes completion of assessments and/or intervention) - Inability to communicate due to severe, uncorrectable hearing loss or speech disorder (if it precludes completion of assessments and/or intervention) - Severe visual impairment (if it precludes completion of assessments and/or intervention) - Inability to read (as it precludes completion of assessments and/or intervention) - Already included in another study sample (e.g. CR cannot also be CCM)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Group 1 (Intervention)
The investigators will evaluate the efficacy of the CC curriculum in a 24-months community-based randomized controlled trial. They will compare changes in CVD-related anthropometric, behavioral, and psychosocial parameters between subjects in intervention and control communities.
Group 2 (Control)
Group 2 will be offered the same activities as Group 1 after the conclusion of the research study.

Locations

Country Name City State
United States Camden and surrounding towns Camden New York
United States Canastota Canastota New York
United States Carthage and surrounding towns Carthage New York
United States Center and Shelbyville Center Texas
United States Groveton and Woodlake Groveton Texas
United States Hamilton and surrounding towns Hamilton New York
United States Littlefield and surrounding towns Littlefield Texas
United States Marshall Marshall Texas
United States Plainview Plainview Texas
United States Rome Rome New York
United States Hounsfield and surrounding towns Sackets Harbor New York
United States Trinity Trinity Texas
United States Watertown Watertown New York

Sponsors (3)

Lead Sponsor Collaborator
Texas A&M University Cornell University, Tufts University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in American Heart Association's Life's Simple 7 (LS7) cardiovascular health score American Heart Association's Life's Simple 7 (LS7) score is a composite of cardiovascular disease (CVD) risk factors (physical activity, eating habits, smoking status, cholesterol, glucose, body mass index (BMI), and blood pressure). Score ranges from 0 to 14. Higher scores indicate better health. Baseline to 24 months
Secondary Change in body mass index (BMI) Height and weight will be self-measured and BMI will be calculated. Baseline to 24 months
Secondary Change in waist circumference Waist circumference (cm(in)) will be self-measured. Baseline to 24 months
Secondary Percent with high/elevated blood pressure Percent with high/elevated blood pressure will be classified from self-reported measurements, diagnosis, and medication use. Baseline to 24 months
Secondary Percent with high/borderline high cholesterol. Percent with high/borderline high cholesterol will be classified from self-reported measurements, diagnosis, and medication use. Baseline to 24 months
Secondary Percent with diabetes/prediabetes Percent with diabetes/ prediabetes will be classified from self-reported measurements, diagnosis, and medication use. Baseline to 24 months
Secondary Change in general health status General health status will be assessed using the general health question from the 36-Item Short Form Survey (SF-36). Scores range from 1 to 5. Higher scores indicate better health. Baseline to 24 months
Secondary Current smoker (y/n) Whether or not a participant currently smokes will be assessed using an LS7 item. Baseline to 24 months
Secondary Change in total HEI score Total Healthy Eating Index (HEI) score will be calculated from a single 24-hour recall collected via the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24). Score ranges from 0 to 100. Higher scores indicate better diet. Baseline to 24 months
Secondary Change in fruit and vegetable intake Total fruit and vegetable intake (cups/day) will be measured using a LS7 item and a 24-hour recall. Baseline to 24 months
Secondary Change in consumption of whole grains Whole grain consumption (servings/day) will be assessed using an LS7 item and a 24-hour recall. Baseline to 24 months
Secondary Change in fiber intake Fiber intake (g/day) will be assessed using the NHANES Dietary Screener Questionnaire (DSQ) and a 24-hour recall. Baseline to 24 months
Secondary Met recommendation for fish consumption (y/n) Whether or not a participant met the recommendation for fish consumption will be assessed using an LS7 item. Baseline to 24 months
Secondary Change in frequency of consuming ultra-processed foods Frequency of ultra-processed foods consumption (times/month) will be assessed using a 9-item questionnaire adapted from the DSQ and the Beverage and Snack Questionnaire (BSQ2) and a 24-hour recall. Baseline to 24 months
Secondary Change in red and processed meat consumption Total red and processed meat consumption (g/week) will be estimated using the DSQ and a 24-hour recall. Baseline to 24 months
Secondary Change in alcohol consumption Alcohol consumption (drinks/day) will be assessed using a 2-item questionnaire adapted from the Alcohol Use Disorders Screening Test (AUDIT) and a 24-hour recall. Baseline to 24 months
Secondary Change in total steps per day Total steps per day will be calculated using the average of self-reported pedometer or wearable fitness tracker readings. Baseline to 24 months
Secondary Change in total physical activity Total physical activity (MET-min/wk) will be assessed using the International Physical Activity Questionnaire long form (IPAQ-long). Baseline to 24 months
Secondary Change in World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR) recommendation adherence score WCRF/AICR recommendation adherence score is a composite of seven items listed above: BMI, physical activity, fiber intake, fruit and vegetable consumption, processed food consumption, red meat consumption, and alcohol consumption. Scores range from 0 to 7. Higher scores indicate greater adherence to the recommendations. Baseline to 24 months
Secondary Change in healthy eating motivation Healthy eating motivation will be assessed by an adapted version of the Naughton & McCarthy Healthy Eating Motivation scale (3 items). Scores range from 1 to 5. Higher scores indicate greater motivation. Baseline to 24 months
Secondary Change in confidence for healthy eating Confidence for healthy eating will also be assessed by using a newly created scale (7 items) adapted from the Sallis Eating Habits Confidence Survey and the Seguin-Fowler Expanded Eating Habits Confidence Survey (7 items). Scores range from 1 to 5. Higher scores indicate greater confidence. Baseline to 24 months
Secondary Change in social support for healthy eating Social support (family and friends) for healthy eating will be assessed by the Ball Social Support for Healthy Eating scale. Scores range from 1 to 5. Higher scores indicate greater social support. Baseline to 24 months
Secondary Change in exercise attitudes Exercise attitudes will be assessed using selected items adapted from section 2, question 5 of the AARP Exercise Attitudes and Behaviors Survey (4 items). Scores range from 1 to 5. Higher scores indicate more positive attitudes. Baseline to 24 months
Secondary Change in exercise confidence Exercise confidence will be assessed by an adapted version of the Sallis Exercise Confidence Survey (3 items). Scores range from 1 to 5. Higher scores indicate greater confidence. Baseline to 24 months
Secondary Change in social support for physical activity Social support (family and friends) for physical activity will be assessed by the Ball Social Support for Physical Activity scale. Scores range from 1 to 5. Higher scores indicate greater social support. Baseline to 24 months
Secondary Change in social engagement Social engagement (family and friends) will be assessed by the Lubben Social Network Scale. Scores range from 1 to 5. Higher scores indicate greater social engagement. Baseline to 24 months
Secondary Change in (community) social cohesion Community social cohesion will be assessed by the social cohesion sub-scale of the Mujahid et al. Neighborhood Environment Scale (NES). Scores range from 1 to 5. Higher scores indicate greater social cohesion. Baseline to 24 months
Secondary Change in individual mobilization Individual mobilization will be assessed using the human capital sub-scale of the Jakes & Shannon Mobilization Scale - Individual. Scores range from 1 to 5. Higher scores indicate greater mobilization. Baseline to 24 months
Secondary Change in general civic engagement attitudes Civic engagement attitudes will be assessed by the attitudes sub-scale of the Doolittle & Faul Civic Engagement Scale. Scores range from 1 to 5. Higher scores indicate more positive civic engagement attitudes. Baseline to 24 months
Secondary Change in general civic engagement behaviors Civic engagement behaviors will be assessed by the behaviors sub-scale of the Doolittle & Faul Civic Engagement Scale. Scores range from 1 to 5. Higher scores indicate more frequent civic engagement behaviors. Baseline to 24 months
Secondary Change in investment in community health Investment in community health (number of priorities) will be assessed using the investment in community health sub-scale of the RWJF National Survey of Health Attitudes. Scores range from 0 to 5. Higher scores indicate higher priority placed on community health. Baseline to 24 months
Secondary Change in walking environment Walking environment will be assessed by an adapted walking sub-scale of the NES (7 items). Scores range from 1 to 5. Higher scores indicate more favorable walking environments. Baseline to 24 months
Secondary Change in neighborhood safety Neighborhood safety will be assessed by an adapted neighborhood safety sub-scale of the NES (3 items). Scores range from 1 to 5. Higher scores indicate greater neighborhood safety. Baseline to 24 months
Secondary Change in neighborhood aesthetic Neighborhood aesthetic quality will be assessed by an adapted neighborhood aesthetic sub-scale of the NES (2 items). Scores range from 1 to 5. Higher scores indicate a more favorable neighborhood. Baseline to 24 months
Secondary Change in fresh fruit and vegetable availability Fresh fruit and vegetable availability will be assessed by an adapted fresh fruit and vegetable availability sub-scale (3 items) of the Green & Glanz Perceived Nutrition Environment Measures Survey (NEMS-P). Scores range from 1 to 5. Higher scores indicate greater availability. Baseline to 24 months
Secondary Change in store selection motivation Store selection motivation will be assessed by an adapted store selection motivation sub-scale from NEMS-P (3 items). Scores range from 1 to 5. Higher scores indicate greater motivation. Baseline to 24 months
Secondary Change in restaurant healthy food availability Restaurant healthy food availability will be assessed by an adapted restaurant healthy food availability sub-scale from NEMS-P (2 items). Scores range from 1 to 5. Higher scores indicate greater availability of healthy food in restaurants. Baseline to 24 months
See also
  Status Clinical Trial Phase
Completed NCT04624412 - Different Intensities of Continuous Aerobic Exercises in Cardiac Rehab Phase 2 N/A
Completed NCT05563701 - Evaluation of the LVivo Image Quality Scoring (IQS)
Recruiting NCT04561908 - Transcatheter Microguidewire Drilling for Transseptal Left Atrial Access N/A
Active, not recruiting NCT06190743 - Perception of Cardiovascular Risk
Completed NCT04562636 - Evaluating a Messaging Campaign in the United States N/A
Completed NCT04580095 - Artificial Intelligence for Improved Echocardiography N/A
Recruiting NCT03277365 - MyGeneRank: A Digital Platform for Next-Generation Genetic Studies N/A
Active, not recruiting NCT05553106 - Evaluation of Cognitive Status, Kinesiophobia, Physical Activity Level, and Functional Performance in Coronary Intensive Care
Completed NCT03429920 - Effect of Fermented Soy Based Product on Cardiometabolic Risk Factors N/A
Recruiting NCT04390672 - Multivessel TALENT N/A
Enrolling by invitation NCT03314818 - Natural History of Carotid Plaque as Determined by 3D Ultrasound N/A
Withdrawn NCT03289104 - Improving Sternal Healing After Cardiac Surgery: Sternal Wire vs ZIPFIX N/A
Completed NCT02917213 - Imaging Silent Brain Infarct And Thrombosis in Acute Myocardial Infarction
Completed NCT02046902 - Developing and Testing a Personalized Evidence-based Shared Decision-making Tool for Stent Selection
Completed NCT01944254 - The Precision of Pulmonary Artery Cardiac Output-measurements in Spontaneously Breathing Patients N/A
Completed NCT01909349 - Web-based Aftercare Intervention for Cardiac Patients N/A
Recruiting NCT01457586 - Hemoderivative Imputable Complications in Initial Uncomplicated Heart Surgery Phase 4
Recruiting NCT01207167 - Mediators of Atherosclerosis in South Asians Living in America
Recruiting NCT01541163 - Heart and Ischemic STrOke Relationship studY N/A
Terminated NCT00968383 - Cardiovascular Magnetic Resonance for the Occluded Infarct-Related Artery Treatment N/A