Obesity
Conditions
Brief summary
With low carbohydrate dietary approach for both arms, the investigators will examine the effectiveness of 12-weeks intensive lifestyle intervention program provided in individual sessions in primary health care obesity clinic in Jeddah with aim to achieve 5% reduction of baseline weight for experimental participants in comparison with active comparator group (only one health education session).
Detailed description
The study has two arms: Active Comparator Arm: Only health education. One session regarding diet restriction and physical activity with printed health education papers. Experimental Arm: Intensive lifestyle intervention Weekly individual session in obesity clinic (15 to 20 min.) for the first 4 weeks then one individual session in obesity clinic (10 to 20 min.) every two weeks (week 5 to week 12). Total sessions in 12 weeks: 8 (including the final data collection visit).The components of the program: 1) Low carbohydrate (aim to achieve spontaneous reduction in calorie intake) 2) increased physical activity; 3) behavioral strategies to facilitate adherence to diet and activity prescriptions.
Interventions
BEHAVIORALIntensive lifestyle intervention
OTHERHealth Education
Sponsors
Saudi Commission for Health Specialties, Saudi Arabia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 20 years old or older * Arabic Male or female * Body mass index in kg/m2 (BMI) ≥30
Exclusion criteria
* Had recent weight loss equal or more than 5% of baseline weight * Currently take weight loss medication or enrolled in another weight loss program * Undergone or scheduled (within study duration) weight loss surgery * History of diabetes, thyroid dysfunction or any other endocrine abnormality, gout, coronary heart disease, stroke, malignancy or psychological condition * Medical condition that limits ability to comply with the program's physical activity recommendations * Pregnant or lactating women * If one participant had recruited in the study, his family members who live with him in the same home will be ineligible (to avoid contamination from the ripple effect on weight loss)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weight Reduction | 1-12 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Waist circumference changes | 1-12 weeks |
| Hip circumference changes | 1-12 weeks |
| Systolic and Diastolic Blood pressure changes | 1-12 weeks |
Outcome results
None listed