Diabetes Clinical Trial
— CBLIOfficial title:
Community-Based Lifestyle and Leadership Intervention for Primary, Secondary, and Tertiary Prevention of Diabetes in Women in the Arab Community
Arab women present increased risk for diabetes, with a 70% greater risk for adult-onset diabetes and a significantly younger age at onset compared with Jewish Israelis. In fact, the rate of diabetes for Arab women in Jerusalem is 4 times higher compared with their Jewish counterparts. Group lifestyle interventions such as the Diabetes Prevention Program (DPP) have documented effectiveness in preventing diabetes; however, many fail to demonstrate outcome maintenance. We predict that integrating leadership skills training into the gold standard DPP would improve the long-term outcome maintenance. Stage 1: A pre-post study design will be utilized, where all community participants will be exposed to intervention components. The sample was selected from pre-existing groups in the local community center, based on their leadership potential. phase 2: The second stage of the trial will not include the leadership component, but instead it will incorporate resiliency training and it aims to evaluate the effect of increased resiliency on the main outcomes including improvement in healthy behaviors such as adherence to Mediterranean diet and as well as a reduction in sedentary lifestyle and increased engagement in physical activity. In addition, resiliency training is likely to improve the maintenance of these behaviors.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | December 31, 2026 |
Est. primary completion date | December 31, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Over age 18 - Able to commit to the intervention timetable Exclusion Criteria: - Younger than age 18 - Unable to commit to the intervention timetable - Were not pregnant with expected delivery during the intervention - Were suffering from other serious mental or physical illness |
Country | Name | City | State |
---|---|---|---|
Israel | Beit-Safafa community center | Jerusalem |
Lead Sponsor | Collaborator |
---|---|
Hadassah Medical Organization |
Israel,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Mediterranean Diet adherence | Will be assessed through Panagiotakos' Mediterranean Diet score (an 11 item self-report measure of adherence to the Mediterranean food pattern) which was adapted to Israeli diet and the Arab culture. Items assessing potato and alcohol consumption were removed and an item assessing nut consumption was added | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Primary | Change in physical activity engagement | Will be assessed through self report of minutes engaged in vigorous and moderate physical via questionnaires. | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Plasma levels of Hemoglobin A1c (HbA1c) | The participants will be referred to their national health insurance in order to conduct a blood test for plasma levels of Hemoglobin A1c (HbA1c) | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Plasma levels of total cholesterol | The participants will be referred to their national health insurance in order to conduct a blood test for plasma levels of total cholesterol | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Plasma levels of HDL | The participants will be referred to their national health insurance in order to conduct a blood test for plasma levels of HDL | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Plasma levels of LDL | The participants will be referred to their national health insurance in order to conduct a blood test for plasma levels of LDL | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Plasma levels of triglycerides | The participants will be referred to their national health insurance in order to conduct a blood test for plasma levels of triglycerides | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Body Mass Index (BMI) | BMI will be calculated by measuring weight and height for each participant. | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Blood Pressure (BP) | Will be measured using standard procedures with an electronic BP apparatus and the recorded measurement is the average of 2 measurements taken in the seated position | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Cardiovascular Disease Knowledge | Will be assessed through self report questionnaire based on the American Heart Association's knowledge survey items | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Stages of Change for targeted health behaviors | Will be assessed through self report questionnaire | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Leadership Self-Efficacy | Will be assessed through self report questionnaire | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Resilience | Resilience will be measured through the validated 10 items Connor-Davidson Resilience Scale (CD-RISC-10) | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Sense of Coherence | Sense of coherence will be measured through the Sense of Coherence 13-item scale | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) | |
Secondary | Change in Self-Rated health | Self reported status of health will be measured using the Self-Rated health questionnaire | Baseline, 6 months after intervention initiation and 6 months following project completion (1 year later) |
Status | Clinical Trial | Phase | |
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