Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT03358797

Community-Based Lifestyle Intervention for Diabetes Prevention in Arab Women

Led by Hadassah Medical Organization · Updated on 2023-04-25

300

Participants Needed

1

Research Sites

522 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Community-Based Lifestyle Intervention for Diabetes Prevention in Arab Women

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Over age 18
  • Able to commit to the intervention timetable
Not Eligible

You will not qualify if you...

  • Younger than age 18
  • Unable to commit to the intervention timetable
  • Not pregnant with expected delivery during the intervention
  • Suffering from other serious mental or physical illness

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beit-Safafa community center

Jerusalem, Israel, 95822

Actively Recruiting

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Research Team

N

Nisreen Agbaria, RN, MSc

CONTACT

D

Donna Zwas, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

4

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