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Individualized Motivational Print Materials to Encourage More Physical Activity

Achieving Physical Activity Guidelines Through an Enhanced Print Intervention

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00367029
Enrollment
256
Registered
2006-08-22
Start date
2006-08-31
Completion date
2011-04-30
Last updated
2014-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Physical Activity

Brief summary

Individuals who are not physically active are at risk for developing heart disease, stroke, and diabetes. Using motivational print materials is one way to encourage individuals to increase their physical activity. This study will evaluate the effect that an enhanced version of an individualized, print-based motivational program has on increasing physical activity among sedentary individuals.

Detailed description

Currently, only 32% of adults in the United States participate in regular physical activity. Several healthcare organizations, including the Centers for Disease Control and Prevention, the National Institutes of Health, and the American Heart Association recommend that adults engage in a minimum of 2 ½ hours of physical activity each week. In a previous study, individuals who received motivational print materials in the mail increased their weekly physical activity more than individuals who received no motivational materials or who received motivational support over the telephone. However, about half of those who were mailed the print materials still did not reach the recommended goal of 2 ½ hours of physical activity per week. The purpose of this study is to compare the effectiveness of an enhanced version of an individualized, print-based motivational program versus a previously tested print-based motivational program at increasing physical activity levels in sedentary individuals. This study will enroll healthy, sedentary individuals. Participants will be randomly assigned to either a print-based, individually tailored motivational program or an enhanced version of the same program. All participants will attend a baseline study visit, which will include body measurements, physical activity assessments, and health and psychological questionnaires. A select group of participants will also take part in an exercise test. Participants will then document their monthly physical activity. Study researchers will use this information, as well as the completed questionnaires, to develop individualized reports, manuals, and tip sheets that include feedback and strategies for increasing physical activity for each participant. Materials will be mailed to participants 14 times throughout the year. Participants in the enhanced intervention will receive additional materials that focus on increasing social support, self regulation, and outcome expectations, as well as materials on how to effectively monitor physical activity levels. They will also attend one study visit to assess their goals with the research staff. At Months 6 and 12, baseline evaluations will be repeated and all participants will be interviewed to assess physical activity levels.

Interventions

BEHAVIORALIndividualized Print-Based Motivational Program

Study researchers will develop individualized reports, manuals, and tip sheets that include feedback and strategies for increasing physical activity for each participant. Materials will be mailed to participants 14 times throughout the year. Participants in the enhanced intervention will receive additional materials that focus on increasing social support, self regulation, and outcome expectations, as well as materials on how to effectively monitor physical activity levels. They will also attend one study visit to assess their goals with the research staff.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
The Miriam Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* In good general health * Sedentary * Able to speak and read English * Planning to live in the area for the duration of the study

Exclusion criteria

* Currently participates in 91 or more minutes of moderate or vigorous physical activity per week * Heart disease * Cerebrovascular disease * Peripheral vascular disease * Chronic obstructive pulmonary disease * Diabetes * High blood pressure * History of gastric bypass surgery * Psychoses * Any serious medical problem that would make exercise unsafe or unwise * Prior participation in a hospital-based or medically supervised weight loss program * Excessive alcohol consumption * Pregnant or plans to become pregnant

Design outcomes

Primary

MeasureTime frame
Achievement of 150 minutes per week of at least moderate intensity physical activityMeasured by the 7-day Physical Activity Recall test at Months 6 and 12

Secondary

MeasureTime frame
Moderators and mediators of the intervention (e.g., motivation and enjoyment)Measured at Months 6 and 12
Cost-effectivenessMeasured at Months 6 and 12

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026