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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: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT02175537
Date of registration: 18/06/2014
Prospective Registration: No
Primary sponsor: Microclinic International
Public title: Microclinic Social Induction Pilot Intervention for Diabetes and Obesity Management in Qatar
Scientific title: Microclinic Social Induction Pilot Intervention for Diabetes and Obesity Management in Qatar
Date of first enrolment: June 2014
Target sample size: 64
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT02175537
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention  
Phase:  N/A
Countries of recruitment
Qatar
Contacts
Name:     Eric L Ding, PhD
Address: 
Telephone:
Email:
Affiliation:  Harvard School of Public Health
Name:     Daniel Zoughbie, DPhil
Address: 
Telephone:
Email:
Affiliation:  Microclinic International
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Behavioral Lifestyle Change
Social Change
Overweight and Obesity
Diabetes Mellitus, Type II
Hypertension
Intervention(s)
Behavioral: Microclinic Social Induction Diabetes and Obesity Program
Primary Outcome(s)
Waist circumference [Time Frame: Baseline, 4th-week midpoint, 7th-week final]
HbA1c [Time Frame: Baseline, end of trial after 7 weeks]
Weight [Time Frame: Weekly measurements between baseline and end of trial after 7 weeks]
Secondary Outcome(s)
Blood Pressure [Time Frame: Baseline, 4th-week midpoint, 7th-week final]
Health Profile Survey [Time Frame: Baseline, end of trial after 7 weeks.]
Secondary ID(s)
NPRP2014-2017
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Qatar Diabetes Association
Harvard School of Public Health
Qatar Supreme Council of Health
Qatar Foundation
Qatar University
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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