Seton Hill University--Personal Empowerment Program

Not Applicable

Completed

• Conditions: Cardiovascular Diseases
• Interventions: Behavioral: health coaching and electronic messaging

• Registration Number: NCT02476604
• Lead Sponsor: Walter Reed National Military Medical Center

Brief Summary

It is widely acknowledged that cardiovascular disease prevention requires intervention as early in the human lifespan as practical. A window of opportunity presents in early adulthood when students gain independence as young adults attending university. In a three-phase investigation, this study will evaluate the behavioral patterns of university students in the domains of diet, exercise, stress management, smoking and sleep (phase 1). Informed with information from phase 1, a pilot study (phase 2) will test the feasibility of performing an intervention in university students consisting of an 8-week period during which the students will receive up to six text messages (by phone or iPad) per week, tailored to address the behavioral issues that the student has identified as needing improvement and for which the student has indicated a desire to make change. Using lessons learned in phase 2, a randomized, controlled trial of the 8 week intervention (phase 3) will compare intervention subjects with controls for outcomes of behavior change, measures of anthropometric data, and serum markers of cardiovascular risk to test the impact of the intervention

Detailed Description

This proposal aims to study the issues of health behaviors in the domains of diet, exercise, stress, and sleep. We aim to improve health behaviors in these domains by evaluating lifestyle choices and communication preferences with a three phase investigation. Phase 1 has the specific objective of lifestyle assessment. Phase 1 will evaluate dietary habits and choices, exercise practices, perceived stress levels, and quantity and timing of sleep utilizing a web-based health survey. The web-based survey tool will populate a secure research database. The data will include demographic information, anthropometric data, actigraphic data to measure exercise levels and sleep time, and laboratory studies that measure glucose metabolism, lipids, and other laboratory markers for cardiovascular risk assessment.

Phase 2 constitutes a pilot study in a limited number of university students to determine the feasibility of causing healthy behavior change with the use of electronic messaging to university students up to six times per week over 8 weeks. Experience from this feasibility study will inform the design of Phase 3.

Phase 3 will measure improvements in the lifestyle behaviors of students as a result of health coaching and electronic feedback messages over an 8 week period comparing their indices of health with a control group that does not receive the coaching and electronic feedback messages. Utilizing lessons learned from Phase 2, subjects randomized to an intervention arm but not subjects randomized to a control arm, will receive health coaching and electronic messages at the rate of up to six times per week over an 8 week period. Before and after this intervention period, measurements of lifestyle choices, anthropometrics, actigraphy for objective exercise and sleep patterns, and cardiac-relevant laboratory studies will be measured. Data from the intervention group will be compared with that of the control group.

Study Timeline

• Study Start: 2012-01
• Primary Completion: 2015-06
• Study Completion: 2015-06
• Study First Submitted: 2015-06-09
• Study First Submitted QC: 2015-06-16
• Study First Posted: 2015-06-19
• Status Verified: 2016-05
• Last Update Submitted: 2016-05-17
• Last Update Posted: 2016-05-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• Full time undergraduate student at Seton Hill University
• Ages 18 to 30 years
• Healthy

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Exclusion Criteria

• Part-time study (less than 12 semester hours of enrollment)
• Under 18 years or over 30 years of age
• Pregnant or planning to become pregnant during study
• Diagnosed eating disorder
• Diagnosed with chronic medical illness such as heart disease (including pacemaker placement), gastro-intestinal disease, diabetes, pulmonary disease
• Taking prescribed medication other than birth control pills or multivitamins on an ongoing basis
• Any condition that may preclude the ability to perform the requirements of the study (for example an orthopedic or neurological condition that prevents the accurate measurement of a subject's height).
• Persons with metal implants (plates, etc)

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Electronic Messaging	health coaching and electronic messaging	Subjects randomized to the intervention arm will receive health coaching and electronic messages at the rate of up to six times per week over an 8 week period.

Primary Outcome Measures

Name	Time	Method
A composite score for adherence to personal goals for Diet, Exercise, Stress Management and Expansion of Sleep Time.	8 weeks	Improvement will be determined by calculating a composite score for % achievement in adhering to goals set for Rate-Your-Plate Dietary Assessment, Exercise Minutes, Stress Reduction by Perceived Stress Scale and Total Sleep Time.

Secondary Outcome Measures

Name	Time	Method
Lipid Profile	8 weeks	Change in chemical profile of lipid panel
Hemoglobin A1C	8 weeks	Change in hemoglobin A1C
Weight Management	8 weeks	BMI and % body fat changes
Glucose Metabolism	8 weeks	Change in fasting glucose

Trial Locations

Locations (2)

Integrative Cardiac Health Project, Walter Reed National Military Medical Center; 🇺🇸 Bethesda, Maryland, United States

Seton Hill University; 🇺🇸 Greensburg, Pennsylvania, United States