Prevention of Weight Gain in University Students (PGP2)
The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2009 by Universitaire de Sherbrooke.
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
Universitaire de Sherbrooke
Collaborators:
Canadian Diabetes Association
Danone Institute
Information provided by:
Universitaire de Sherbrooke
ClinicalTrials.gov Identifier:
NCT00995462
First received: October 14, 2009
Last updated: NA
Last verified: October 2009
History: No changes posted
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Purpose
This study assess whether a small-group seminar intervention to prevent weight gain is effective in a general university student population, and to address the relative role of biological vs. lifestyle factors in predicting weight gain in humans.
| Condition | Intervention |
|---|---|
|
Prevention Weight Gain |
Behavioral: Lifestyle intervention seminars |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Prevention of Weight Gain in University Students |
Further study details as provided by Universitaire de Sherbrooke:
Primary Outcome Measures:
- Weight change [ Time Frame: 2 years ] [ Designated as safety issue: No ]
| Enrollment: | 319 |
| Study Start Date: | September 2006 |
| Estimated Study Completion Date: | October 2011 |
| Estimated Primary Completion Date: | October 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| No Intervention: Control | |
| Experimental: Small-group seminar for 2 years |
Behavioral: Lifestyle intervention seminars
The first sessions emphasize acquisition of new knowledge during interactive group seminars designed to maximize attendant's participation by adapting wellknown quiz-show or parlour games to deliver key concepts. A number of sessions are aimed at increasing self-efficacy through problem-solving, time-management strategies, individual self monitoring and goal-setting.During the second year, the intervention focuses on maintenance of healthy behaviour with empowerment of the participants using problem-solving, goal-setting, planning, and self-monitoring skills.
|
| Experimental: Small-group seminars for 1 year followed by email intervention |
Behavioral: Lifestyle intervention seminars
The first sessions emphasize acquisition of new knowledge during interactive group seminars designed to maximize attendant's participation by adapting wellknown quiz-show or parlour games to deliver key concepts. A number of sessions are aimed at increasing self-efficacy through problem-solving, time-management strategies, individual self monitoring and goal-setting.During the second year, the intervention focuses on maintenance of healthy behaviour with empowerment of the participants using problem-solving, goal-setting, planning, and self-monitoring skills.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- First year students at the Université de Sherbrooke.
Exclusion Criteria:
- Presence of diseases or medications that would be expected to affect weight (cystic fibrosis, diabetes, inflammatory bowel diseases, anorexia nervosa, bulimia, etc.).
- Pregnancy or planning a pregnancy in the next two years.
- Unable to give an informed consent.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00995462
Locations
| Canada, Quebec | |
| Université de Sherbrooke | |
| Sherbrooke, Quebec, Canada, J1K 2R1 | |
Sponsors and Collaborators
Universitaire de Sherbrooke
Canadian Diabetes Association
Danone Institute
Investigators
| Principal Investigator: | Marie-France Langlois, MD | Universitaire de Sherbrooke |
More Information
No publications provided by Universitaire de Sherbrooke
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Marie-France Langlois, Principal Investigator, Université de Sherbrooke |
| ClinicalTrials.gov Identifier: | NCT00995462 History of Changes |
| Other Study ID Numbers: | 05-025 |
| Study First Received: | October 14, 2009 |
| Last Updated: | October 14, 2009 |
| Health Authority: | Canada: Health Canada |
Additional relevant MeSH terms:
|
Weight Gain Body Weight Changes Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013