Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT02175537 |
Date of registration:
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18/06/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Microclinic Social Induction Pilot Intervention for Diabetes and Obesity Management in Qatar
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Scientific title:
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Microclinic Social Induction Pilot Intervention for Diabetes and Obesity Management in Qatar |
Date of first enrolment:
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June 2014 |
Target sample size:
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64 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT02175537 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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Phase:
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N/A
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Countries of recruitment
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Qatar
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Contacts
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Name:
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Eric L Ding, PhD |
Address:
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Telephone:
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Email:
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Affiliation:
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Harvard School of Public Health |
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Name:
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Daniel Zoughbie, DPhil |
Address:
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Telephone:
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Email:
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Affiliation:
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Microclinic International |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Over 18 years old
- Mentally competent
- Body Mass Index of 30 or higher
- Body Mass Index of 25 or higher and self-reported pre-diabetes or type II diabetes
Exclusion Criteria:
- They do not meet the above criteria
- They are pregnant
- They have significant medical complications that prevent them from making changes to
diet or level of physical activity.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Behavioral Lifestyle Change
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Social Change
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Overweight and Obesity
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Diabetes Mellitus, Type II
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Hypertension
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Intervention(s)
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Behavioral: Microclinic Social Induction Diabetes and Obesity Program
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Primary Outcome(s)
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Waist circumference
[Time Frame: Baseline, 4th-week midpoint, 7th-week final]
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HbA1c
[Time Frame: Baseline, end of trial after 7 weeks]
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Weight
[Time Frame: Weekly measurements between baseline and end of trial after 7 weeks]
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Secondary Outcome(s)
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Blood Pressure
[Time Frame: Baseline, 4th-week midpoint, 7th-week final]
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Health Profile Survey
[Time Frame: Baseline, end of trial after 7 weeks.]
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Secondary ID(s)
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NPRP2014-2017
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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