- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01075139
Brief Motivational Intervention to Increase Physical Activity and Fruit/Vegetable Intake
September 20, 2011 updated by: Matthew P. Martens, University of Missouri-Columbia
Pilot Trial of a Brief Motivational Intervention to Increase Physical Activity and Fruit/Vegetable Intake Among College Students
Research has shown that a high percentage of college students do not meet recommended national guidelines for physical activity or fruit/vegetable intake.
The purpose of this study was to pilot test the short-term efficacy of a one-on-one, brief motivational intervention (BMI) designed to increase physical activity and fruit/vegetable intake.
It was hypothesized that participants in the BMI condition would report greater physical activity and fruit/vegetable intake at follow-up than those in an education-only control condition.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Tennessee
-
Memphis, Tennessee, United States, 38152
- University of Memphis
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Two or fewer days of 30+ minutes of moderate physical activity per week
- Zero days of 20+ minutes of vigorous physical activity per week
Exclusion Criteria:
- Three or more days of 30+ minutes of moderate physical activity per week
- One or more days of 20+ minutes of vigorous physical activity per week
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Brief Motivational Intervention
Subjects in this condition met one-on-one with a counselor for 30 minutes.
Subjects received personalized feedback regarding their current physical activity levels and fruit/vegetable intake.
Counselors used a motivational interviewing style to try to help resolve ambivalence about changing their current behaviors.
|
30 minute one-on-one meeting
|
Active Comparator: Educational information
Subjects in this condition received general educational information about the benefits associated with physical activity and fruit/vegetable intake.
|
Educational handouts/brochures
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Vigorous physical activity minutes per week.
Time Frame: One-month follow-up.
|
One-month follow-up.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Moderate physical activity minutes per week.
Time Frame: One-month follow-up.
|
One-month follow-up.
|
|
Fruit and vegetable intake per week
Time Frame: One-month follow-up
|
Number of fruit and vegetable servings per day per week
|
One-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Matthew P Martens, Ph.D., University of Missouri-Columbia
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2008
Primary Completion (Actual)
October 1, 2009
Study Completion (Actual)
October 1, 2009
Study Registration Dates
First Submitted
February 23, 2010
First Submitted That Met QC Criteria
February 23, 2010
First Posted (Estimate)
February 24, 2010
Study Record Updates
Last Update Posted (Estimate)
September 22, 2011
Last Update Submitted That Met QC Criteria
September 20, 2011
Last Verified
September 1, 2011
More Information
Terms related to this study
Other Study ID Numbers
- N/A (unfunded trial)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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