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Examining Two Print-based Exercise Interventions for Women (WWP)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01203215
First Posted: September 16, 2010
Last Update Posted: November 7, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
The Miriam Hospital
Information provided by:
Temple University
  Purpose
Print-based interventions, specifically interventions that are theoretically-based have been shown to be effective for individuals. These types of interventions are of particular importance for those individuals who, due to transportation, work, family, social, or financial demands have difficulty participating in face-to-face programs. Therefore, we decided to test 2 such print based programs for women.

Condition Intervention Phase
Physical Activity Behavior Behavioral: 2 print based physical activity interventions Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Evaluating Self-Help Programs for Exercise Adoption and Maintenance in Women

Resource links provided by NLM:


Further study details as provided by Temple University:

Primary Outcome Measures:
  • Physical activity [ Time Frame: 3 months ]

Secondary Outcome Measures:
  • physical activity [ Time Frame: 12 months ]

Enrollment: 280
Study Start Date: June 2002
Study Completion Date: December 2005
Primary Completion Date: June 2005 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: JumpStart Behavioral: 2 print based physical activity interventions
physical activity promotion
Experimental: Choose to Move Behavioral: 2 print based physical activity interventions
physical activity promotion
Active Comparator: Wellness Behavioral: 2 print based physical activity interventions
physical activity promotion

Detailed Description:
We conducted a randomized controlled trial in which participants were randomly assigned to one of three groups: (1) Choose to Move (CTM), a gender-targeted intervention (2) Jumpstart, a motivationally-tailored print-based intervention, or (3) Wellness contact control group. Objective and self-report measures of physical activity and psychosocial mediators of change were assessed at 3 months to evaluate the efficacy of the programs and maintenance of these programs will be conducted by examining a 9 month follow-up phase. This design allows a direct comparison between two print-based physical activity self-help programs. The use of non face-to-face interventions is critical to reach the large numbers of women in United States who are not physically active. Tailored print materials (i.e., Jumpstart) will enable participants to have information that is matched to their level of motivation, and thus might be expected to be more efficacious than a standard self-help intervention.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • healthy women
  • sedentary

Exclusion Criteria:

  • participating in > 90 minutes of purposeful physical activity (e.g., walking, cycling).
  • medical problems that could potentially impede or exacerbated by physical activity
  • history of coronary heart disease
  • myocardial infraction
  • symptoms of angina
  • stroke
  • diabetes
  • osteoporosis
  • osteoarthritis
  • severe orthopedic problems.
  • a planned move from the area within the next year
  • current or planned pregnancy
  • hospitalization for a psychiatric disorder within the last 3 years
  • current suicidal or psychotic episodes
  • currently using certain prescription medication such as beta blockers for hypertension
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01203215


Locations
United States, Rhode Island
The Miriam Hospital
Providence, Rhode Island, United States, 02903
Sponsors and Collaborators
Temple University
The Miriam Hospital