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Prevention of Weight Gain in University Students

Prevention of Weight Gain in University Students

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00995462
Acronym
PGP2
Enrollment
319
Registered
2009-10-15
Start date
2006-09-30
Completion date
2011-12-31
Last updated
2013-12-11

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

Conditions

Prevention, Weight Gain

Brief summary

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.

Interventions

BEHAVIORALLifestyle 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.

Sponsors

Canadian Diabetes Association
CollaboratorOTHER
Danone Institute
CollaboratorUNKNOWN
Marie-France Hivert
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
Weight change2 years

Countries

Canada

Outcome results

None listed

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