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12 Weeks Intensive Lifestyle Intervention Program in Primary Care Obesity Clinic for Obese Adults: Jeddah 2015

Not Applicable
Conditions
Obesity
Interventions
Behavioral: Intensive lifestyle intervention
Other: Health Education
Registration Number
NCT02464566
Lead Sponsor
Saudi Commission for Health Specialties, Saudi Arabia
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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
140
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)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
L GroupHealth EducationWeekly 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) behavioural strategies to facilitate adherence to diet and activity prescriptions.
L GroupIntensive lifestyle interventionWeekly 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) behavioural strategies to facilitate adherence to diet and activity prescriptions.
C GroupHealth EducationOne session regarding diet restriction and physical activity with printed health education papers.
Primary Outcome Measures
NameTimeMethod
Weight Reduction1-12 weeks
Secondary Outcome Measures
NameTimeMethod
Waist circumference changes1-12 weeks
Hip circumference changes1-12 weeks
Systolic and Diastolic Blood pressure changes1-12 weeks
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