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Completed

NCT Number: NCT00242658

Computerized Health Education to Promote Physical Activity

This study will test the efficacy of providing primary care physicians and their patients with computer-tailored information, based on patients' responses to survey questions. The health education messages are designed to encourage patients to become physically active and to encourage physicians to counsel their patients about exercise.

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Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Jefferson Family Medicine Associates, Philadelphia, Pennsylvania, United States

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About this study

The main objective of this study is to determine, via a 6-month randomized controlled study, the efficacy of providing tailored physical activity computer reports to patients and physicians. The primary outcome is minutes of physical activity measured by the 7-Day Physical Activity Recall interview at 6 months. The intervention group completed physical activity surveys at baseline, 1, 3, and 6 months. Based on their responses, participants received four feedback reports at each time point. The reports aimed to motivate participants to increase physical activity, personalized to participants' needs; they also included an activity prescription. The control group received identical procedures, except that they received general reports on preventive screening based on their responses to preventive screening questions.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Ability to speak and read English
  • Current patient of a physician participating in this study (if selecting a new physician, may deliberately select one that is involved in the study, in order to participate)
  • Ability to complete all written surveys
  • Accessible for follow-up telephone surveys
  • Ability to undergo exercise testing

Exclusion criteria

  • Currently participating in another research study
  • Planning to move out of the Philadelphia area
  • Unable to walk without pain
  • Pregnant or planning to become pregnant in the year following study entry
  • Excessive drinking
  • Coronary heart disease
  • Congestive heart failure
  • Peripheral vascular disease
  • Cerebrovascular disease
  • Chronic obstructive pulmonary disease
  • Arrhythmia
  • Recurrent seizures
  • Dizziness
  • Balance problems
  • Psychoses

Treatment and study plan

Tailored Physical Activity Intervention

Behavioral

Tailored physical activity computer reports will be provided to patients and physicians.

Other names: Exercise Intervention

Primary outcomes

  1. 7-Day Physical Activity Recall (7-Day PAR)

    Time frame: 6 months

    Minutes of physical activity measured by the 7-Day Physical Activity Recall (7-Day PAR), which is an interviewer-administered self-report physical activity measure of minutes spent in moderate and vigorous intensity leisure and non-leisure activities over the preceding 7 days. It was administered to study participants at baseline and 6 months.

Secondary outcomes

  1. Change in Behavioral Processes of Change Between Baseline and 6 Months

    Time frame: Baseline and 6 months

    Behavioral processes were assessed by asking participants to rate their responses to 24 statements on a Likert scale (1 = never to 5 = repeatedly) to statements such as, "I tell myself I am able to be physically active if I want to. To create the overall measure, individual items are averaged. Higher numbers represent greater use of behavioral processes of change, so that the overall scale retains a maximum of 5.0 and minimum value of 1.0. The scale values are not numerical, they represent scores on the scale, where 5=repeatedly and 1=never.

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • Thomas Jefferson University

Registry information

Official study title

Computerized Physical Activity Promotion in Primary Care

Important dates

Study start
2005
Primary completion
2007
Study completion
2008
First posted
Oct 20, 2005
Registry last updated
Nov 12, 2012

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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