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OpenTrials
Completed

NCT Number: NCT00731094

The VA-STRIDE Study

The purpose of the study was to examine the effectiveness of an expert-system, print-based physical activity (PA) intervention delivered to Veterans receiving primary care at the VA Pittsburgh Healthcare System (VAPHS).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA

Pittsburgh, Pennsylvania, 15240, United States

About this study

A.1 The primary aim of the study was to determine the effect of a physical activity intervention designed to increase physical activity for sedentary Veterans at VAPHS.

A.2. Secondary aims were to assess key health-related outcomes related to the intervention including health and quality of life. The specific outcomes were to (a) estimate the impact of the intervention on physical function, health-related quality of life (HRQL), weight, blood pressure, and serum lipids; and (b) characterize variation in intervention effectiveness by participant sociodemographic and health characteristics, such as age, race, and baseline health status.

232 Veterans were randomized to either the physical activity intervention group or the attention control group. Participants randomized to the physical activity intervention group participated in an individualized physical activity counseling session at baseline, conducted by an exercise physiologist, with guided goal setting to increase physical activity gradually to at least 150 minutes/week of moderate intensity. An additional 14 intervention counseling contacts, generated by participants' responses to physical activity questionnaires and individually tailored computer-generated expert system feedback messages based on stages of the motivational readiness for change model, were conducted via postal mail over the subsequent 12 months in parallel with routine primary care. Newsletters providing additional support and suggestions for increasing physical activity were also part of the mailed counseling contacts. Participants randomized to the attention control group participated in a generalized healthy lifestyle counseling session at baseline, conducted by a health educator, which included limited advice to become more physically active. Fourteen follow-up wellness newsletters that focused on healthy lifestyle issues other than physical activity were sent to participants via postal mail over the subsequent 12 months with the same frequency of contact as for the physical activity intervention group and in parallel with routine primary care. Assessment of effectiveness occurred at baseline, 6, and 12 months.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • at least 18 years of age at the time of enrollment,
  • one or more primary care clinic visits at VAPHS in the 12 months prior to enrollment
  • overweight or obese, with a BMI > =25.0 kg/m^2 at the most recent primary care visit prior to enrollment.

Exclusion criteria

  • primary care provider judgment that unsupervised moderate-intensity exercise will place the Veteran at risk of a cardiovascular event, or other safety concern for guided but unsupervised physical activity
  • Veteran is nonambulatory or requires assistive devices to ambulate (e.g., wheelchairs, prosthetic legs, canes or walkers),
  • Veteran regularly participates in moderate to brisk physical activity 60 minutes or more each week
  • current diagnosis of pulmonary hypertension, chronic obstructive pulmonary disease (COPD), and other comorbid conditions deemed to be contraindications for guided, unsupervised physical activity
  • self-reported blindness and/or unable to read printed material in English (e.g., a newspaper)
  • plans to move from the VAPHS treatment area in the next 12 months
  • unable or unwilling to travel to the study site 4 times during the 12-month study period
  • VAPHS employee
  • current participant in another interventional research study that may confound outcomes
  • unable or unwilling to provide signed, informed consent

Treatment and study plan

Expert system-based physical activity counseling

Behavioral

The intervention included 14 mailings to participants that involved completion of physical activity questionnaires printed on forms that were 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 were also part of the mailing program.

Primary outcomes

  1. Moderate Intensity Physical Activity: Modified Community Healthy Activities Model Program for Seniors (CHAMPS) Questionnaire

    Time frame: Month 0

    Participants achieving 150 minutes/week of moderate intensity or greater physical activity at Month 0 as measured with the modified CHAMPS Questionnaire

  2. Moderate Intensity Physical Activity: Modified CHAMPS Questionnaire

    Time frame: Month 6

    Participants achieving 150 minutes/week of moderate intensity or greater physical activity at Month 6 as measured with the modified CHAMPS Questionnaire

  3. Moderate Intensity Physical Activity: Modified CHAMPS Questionnaire

    Time frame: Month 12

    Participants achieving 150 minutes/week of moderate intensity or greater physical activity at Month 12 as measured with the modified CHAMPS Questionnaire

  4. Moderate Intensity Physical Activity: Accelerometer

    Time frame: Month 0

    Participants with an average of at least 30 minutes/day of moderate intensity or greater physical activity in a subset of the study population for whom accelerometer data were obtained: 97 of 116 in Physical Activity Intervention Group and 103 of 116 in Attention Control Group at Month 0

  5. Moderate Intensity Physical Activity: Accelerometer

    Time frame: Month 6

    Participants with an average of at least 30 minutes/day of moderate intensity or greater physical activity in a subset of the study population for whom accelerometer data were obtained: 77 of 101 in Physical Activity Intervention Group and 76 of 107 in Attention Control Group in Month 6

  6. Moderate Intensity Physical Activity: Accelerometer

    Time frame: Month 12

    Participants with an average of at least 30 minutes/day of moderate intensity or greater physical activity in a subset of the study population for whom accelerometer data were obtained: 71 of 98 in Physical Activity Intervention Group and 74 of 105 in Attention Control Group at Month 12

Secondary outcomes

  1. Weight

    Time frame: Month 0

    Weight in kilograms (kg) measured at Month 0

  2. Weight

    Time frame: Month 6

    Weight in kilograms at measured at Month 6

  3. Weight

    Time frame: Month 12

    Weight in kilograms measured at Month 12

  4. Systolic Blood Pressure (BP)

    Time frame: Month 0

    Systolic BP in millimeters of mercury (mmHg) measured at Month 0

  5. Systolic BP

    Time frame: Month 6

    Systolic BP measured at Month 6

  6. Systolic BP

    Time frame: Month 12

    Systolic BP measured at Month 12

  7. Diastolic BP

    Time frame: Month 0

    Diastolic BP measured at Month 0

  8. Diastolic BP

    Time frame: Month 6

    Diastolic BP measured at Month 6

  9. Diastolic BP

    Time frame: Month 12

    Diastolic BP measured at Month 12

  10. Low-density Lipoprotein (LDL) Cholesterol

    Time frame: Month 0

    LDL cholesterol in milligrams per deciliter (mg/dL) measured at Month 0

  11. LDL Cholesterol

    Time frame: Month 6

    LDL cholesterol measured at Month 6

  12. LDL Cholesterol

    Time frame: Month 12

    LDL cholesterol measured at Month 12

  13. High-density Lipoprotein (HDL) Cholesterol

    Time frame: Month 0

    HDL cholesterol in milligrams/deciliter (mg/dL) measured at Month 0

  14. HDL Cholesterol

    Time frame: Month 6

    HDL cholesterol measured at Month 6

  15. HDL Cholesterol

    Time frame: Month 12

    HDL cholesterol measured at Month 12

  16. Triglycerides

    Time frame: Month 0

    Triglycerides measured at Month 0

  17. Triglycerides

    Time frame: Month 6

    Triglycerides measured at Month 6

  18. Triglycerides

    Time frame: Month 12

    Triglycerides measured at Month 12

  19. Health Related Quality of Life (HRQL): Short Form 36 Health Survey Questionnaire (SF-36) Physical Component Summary Measure (PCS)

    Time frame: Month 0

    HRQL: SF-36 PCS measured at Month 0. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The PCS aggregates the scales for bodily pain, general health perceptions, physical functioning, and role limitation due to physical health problems.

  20. HRQL: SF-36 PCS

    Time frame: Month 6

    HRQL: SF-36 PCS measured at Month 6. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The PCS aggregates the scales for bodily pain, general health perceptions, physical functioning, and role limitation due to physical health problems.

  21. HRQL: SF-36 PCS

    Time frame: Month 12

    HRQL: SF-36 PCS measured at Month 12. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The PCS aggregates the scales for bodily pain, general health perceptions, physical functioning, and role limitation due to physical health problems.

  22. HRQL: SF-36 Mental Component Summary Measure (MSC)

    Time frame: Month 0

    HRQL: SF-36 MCS measured at Month 0. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The MCS aggregates the scales for vitality, mental health, social functioning, and role limitations due to personal or emotional problems.

  23. HRQL: SF-36 MCS

    Time frame: Month 6

    HRQL: SF-36 MCS measured at Month 6. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The MCS aggregates the scales for vitality, mental health, social functioning, and role limitations due to personal or emotional problems.

  24. HRQL: SF-36 MCS

    Time frame: Month 12

    HRQL: SF-36 MCS measured at Month 12. The SF-36 is a multi-purpose, short-form health survey with 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. The 8 scales are the weighted sums of the 2-10 questions in their section. Norm-based scoring, where each scale and component summary measures were scored to have the same average (50) and the same standard deviation (10 points), was used for reporting results in this study. Scores are interpreted as the lower the score the more disability; conversely, the higher the score the less disability. The MCS aggregates the scales for vitality, mental health, social functioning, and role limitations due to personal or emotional problems.

  25. Physical Function: 6-Minute Walking Distance (6MWD)

    Time frame: Month 0

    Physical Function: 6MWD in meters measured at Month 0

  26. Physical Function: 6MWD

    Time frame: Month 6

    Physical Function: 6MWD measured at Month 6

  27. Physical Function: 6MWD

    Time frame: Month 12

    Physical Function: 6MWD measured at Month 12

Sponsors and collaborators

Lead sponsor

US Department of Veterans Affairs

Fed

Collaborators

  • Brown University
  • University of Pittsburgh

Registry information

Official study title

Expert System-Based Feedback in Sedentary Overweight Veterans

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Aug 8, 2008
Registry last updated
Apr 27, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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