Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes
NCT ID: NCT01814995
Last Updated: 2014-09-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
36 participants
INTERVENTIONAL
2012-01-31
2013-09-30
Brief Summary
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Detailed Description
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The investigators will hold in-person sessions at a frequency of once per month over a 4-month period. In addition to the in-person, on-site sessions, we will arrange for participants to have in a grocery store 'tour' led by a student from the McGill School of Dietetics and Human Nutrition BSc program. This will allow a review of label reading and interpretation as well as tips on produce selection. Details of the intervention are provided under the trial arm section below.
Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Nutrition/Physical Activity Intervention
There will be four in-person group sessions (1/month), two including the participants' partners, and all with on-site child care. Sessions will include preparation of a healthy meal (hands-on) and discussions of mindful eating, balanced meals, portion sizes, and preparing food at home, under a dietitian's supervision. Sessions will also include a one-hour physical activity information/practice session with a kinesiologist. Participants will track daily step counts with a pedometer and aim to eventually reach more than 10,000 steps/day. They will also receive instruction and demonstration from a kinesiologist of some simple resistance exercises they may perform at home. Between sessions, participants will receive advice and support through a study-specific website and telephone calls.
Nutrition/Physical Activity Intervention
Please see Arm description.
Interventions
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Nutrition/Physical Activity Intervention
Please see Arm description.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Body mass index (BMI) ≥ 24 kg/m2
3. Ability to speak and read English or French
Exclusion Criteria
2. Type 2 diabetes
3. Use of antihyperglycemic medication
4. Pregnant or planning to become pregnant again in the next year
5. Food allergies
6. Chronic condition/ medications that could impact weight (e.g. malignancy, weight loss medications, anti-depressants)
7. Current smoker
18 Years
55 Years
FEMALE
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
McGill University Health Centre/Research Institute of the McGill University Health Centre
OTHER
Responsible Party
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Kaberi Dasgupta, MD, MSc, FRCP (C)
Associate Professor, McGill University
Principal Investigators
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Kaberi Dasgupta, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
McGill University and McGill University Health Centre
Locations
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McGill University Health Centre
Montreal, Quebec, Canada
Sir Mortimer Davis Jewish General Hospital
Montreal, Quebec, Canada
Countries
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References
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Dasgupta K, Da Costa D, Pillay S, De Civita M, Gougeon R, Leong A, Bacon S, Stotland S, Chetty VT, Garfield N, Majdan A, Meltzer S. Strategies to optimize participation in diabetes prevention programs following gestational diabetes: a focus group study. PLoS One. 2013 Jul 4;8(7):e67878. doi: 10.1371/journal.pone.0067878. Print 2013.
Leong A, Rahme E, Dasgupta K. Spousal diabetes as a diabetes risk factor: a systematic review and meta-analysis. BMC Med. 2014 Jan 24;12:12. doi: 10.1186/1741-7015-12-12.
Brazeau AS, Leong A, Meltzer SJ, Cruz R, DaCosta D, Hendrickson-Nelson M, Joseph L, Dasgupta K; MoMM study group. Group-based activities with on-site childcare and online support improve glucose tolerance in women within 5 years of gestational diabetes pregnancy. Cardiovasc Diabetol. 2014 Jun 30;13:104. doi: 10.1186/1475-2840-13-104.
Related Links
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Main results
related systematic review (spousal diabetes concordance)
Focus group study that informed intervention design
Other Identifiers
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CIHR-CAI117789
Identifier Type: -
Identifier Source: org_study_id
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