Improving treatment adherence for metabolic health in Negev Bedouins
Examining the Effectiveness of Family and Community-Based Intervention Programs to Improve Treatment Adherence for Overweight, Obesity, Prediabetes, Metabolic Syndrome, and Type 2 Diabetes in the Bedouin Community in the Negev
NA · Ariel University · NCT06575465
This study is testing a family-focused program to help Bedouins in the Negev stick to a healthier lifestyle to better manage type 2 diabetes and obesity.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 170 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Ariel University (other) |
| Locations | 1 site (Rahat) |
| Trial ID | NCT06575465 on ClinicalTrials.gov |
What this trial studies
This study evaluates a family-centered intervention program aimed at improving treatment adherence for metabolic health among the Bedouin community in the Negev, which faces high rates of type 2 diabetes and obesity. The intervention consists of 10 sessions over 12 months focusing on nutrition, physical activity, and cultural aspects to promote adherence to a Mediterranean diet. Participants will be assessed for changes in fasting glucose, HbA1c, lipid profiles, BMI, physical activity, and quality of life. The study employs a controlled community intervention design with two groups: one receiving the intervention and the other serving as a control.
Who should consider this trial
Good fit: Ideal candidates include Bedouin men and women aged 18 and above who are diagnosed with overweight, obesity, metabolic syndrome, prediabetes, or type 2 diabetes.
Not a fit: Patients with other chronic diseases that may interfere with the study or those who are pregnant or lactating may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve metabolic health outcomes and treatment adherence in the Bedouin community.
How similar studies have performed: Other studies have shown success with community-based participatory approaches in improving health outcomes, suggesting potential for this culturally tailored intervention.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Bedouin men and women aged 18 and above * Diagnosed with overweight, obesity, metabolic syndrome, prediabetes, or type 2 diabetes * Consent to participate in the study Exclusion Criteria: * Individuals with other chronic diseases that might interfere with the study * Pregnant or lactating women * Individuals unable to provide informed consent
Where this trial is running
Rahat
- Clalit healthcare clinic — Rahat, Israel (RECRUITING)
Study contacts
- Principal investigator: Muflah Ataika, MD — Rahat Counseling Clinic, Southern District, Clalit Health Services.
- Study coordinator: Vered Kaufman-Shriqui, PhD
- Email: veredks@ariel.ac.il
- Phone: +972587751199
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Community-Based Participatory Research, Type 2 Diabetes Mellitus, Obesity, Community based participatory research, Health promotion, Clinical trial, Prediabetes