The VA-STRIDE Study
| Tracking Information | |||||
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| First Received Date ICMJE | August 5, 2008 | ||||
| Last Updated Date | April 3, 2013 | ||||
| Start Date ICMJE | June 2010 | ||||
| Estimated Primary Completion Date | April 2013 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Physical activity [ Time Frame: 12 months ] [ Designated as safety issue: No ] The primary outcome of the study is a comparison of participant-specific responses to the Community Healthy Activity Model Program for Seniors (CHAMPS) Questionnaire at Baseline, 6-Months, and 12-Months. Seven-day accelerometer data collected at the same timepoints will supplement the CHAMPS. |
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| Original Primary Outcome Measures ICMJE |
Physical activity [ Time Frame: 12 months ] [ Designated as safety issue: No ] | ||||
| Change History | Complete list of historical versions of study NCT00731094 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | The VA-STRIDE Study | ||||
| Official Title ICMJE | Expert System-Based Feedback in Sedentary Overweight Veterans | ||||
| Brief Summary | The purpose of the study is to examine the effectiveness and cost-utility of an expert-system, print-based physical activity intervention delivered to Veterans receiving primary care at the VA Pittsburgh Healthcare System. |
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| Detailed Description | A.1 The primary aim of the study is to determine the effect of a physical activity intervention designed to increase physical activity for sedentary Veterans at the VA Pittsburgh Healthcare System. A.2. Secondary aims are to assess key health-related outcomes related to the intervention including health and quality of life. The specific outcomes are to (a) estimate the impact of the intervention on physical function, health-related quality of life (HRQL), weight, blood pressure and serum lipids; (b) characterize variation in intervention effectiveness by participant sociodemographic and health characteristics, such as age, race, and baseline health status; and (c) estimate cost-per-Quality Adjusted Life Year (QALY) at 12 months. Up to 300 Veterans will be randomized to intervention or control groups. Participants must have a self-reported sedentary lifestyle and a body mass index (BMI) >= 25.0 kg/m2. Those randomized to the intervention will receive a 12-month intervention that involves completion of physical activity questionnaires printed on forms that will be scanned into a computerized expert system program to generate individually-tailored feedback messages. Those randomized to the control will receive limited advice at baseline from a health educator to become more physically active, followed by routine primary care for 12 months with an attention control focused on healthy lifestyle issues other than physical activity. Assessment of effectiveness will occur at baseline, 6, and 12 months. Cost analyses will be performed from a payer perspective. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE |
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| Intervention ICMJE | Behavioral: Expert system-based physical activity counseling
The intervention will include 14 mailings to participants that involve completion of physical activity questionnaires printed on forms that will be scanned into a computerized expert system program to generate individually-tailored feedback messages and related manuals based on the Stages of Motivational Readiness for Change Model. Newsletters providing additional support and suggestions for increasing physical activity also will be part of the mailing program. |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Active, not recruiting | ||||
| Enrollment ICMJE | 232 | ||||
| Estimated Completion Date | June 2013 | ||||
| Estimated Primary Completion Date | April 2013 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00731094 | ||||
| Other Study ID Numbers ICMJE | IIR 07-154 | ||||
| Has Data Monitoring Committee | Yes | ||||
| Responsible Party | Department of Veterans Affairs | ||||
| Study Sponsor ICMJE | Department of Veterans Affairs | ||||
| Collaborators ICMJE |
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| Investigators ICMJE |
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| Information Provided By | Department of Veterans Affairs | ||||
| Verification Date | April 2013 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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