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Evaluation of a Socio-ecological Cardiovascular Disease Prevention Intervention for Ultra-Orthodox Jewish Hasidic Women

Evaluation of a Socio-ecological Cardiovascular Disease Prevention Intervention for Ultra-Orthodox Jewish Hasidic Women Using a Participatory Approach

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03201523
Enrollment
239
Registered
2017-06-28
Start date
2013-11-01
Completion date
2025-12-31
Last updated
2023-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Health Behavior

Keywords

Community-based Intervention, Socio-ecological Model, Participatory Approach, Ultra-Orthodox Jewish women

Brief summary

The purpose of this research study is to design, implement, and evaluate a community level, socio-ecological based CVD prevention intervention using a participatory approach for women in a homogeneous ultra-Orthodox Jewish Hasidic community in Israel. A quasi-experimental, pre-post study design will be utilized, where all community participants will be exposed to intervention components. Pre and post samples will be selected through randomized cluster sampling of pre-existing community groups. It is hypothesized that ultra-Orthodox Jewish Hasidic women exposed to this community intervention will have improved healthy eating behaviors, reduced unhealthy eating behaviors, increased engagement in physical activity and sleep, and reduced risk for obesity (weight, BMI).

Detailed description

The purpose of this research study is to design, implement, and evaluate a community level, socio-ecological based CVD prevention intervention using a participatory approach for women in a homogeneous ultra-Orthodox Jewish Hasidic community in Israel. A quasi-experimental, pre-post study design will be utilized, where all community participants will be exposed to intervention components. Pre and post samples will be selected through randomized cluster sampling of pre-existing community groups (n=239 ). Intervention components will be designed through qualitative and quantitative data collection (focus groups, interviews, and questionnaires) from the target population and implementation will be conducted in partnership with community organizations. Intervention components will include a health newsletter, health workshops, community evening/health project registration, lay leader training, neighborhood exercise groups, community walking programs with pedometers, healthy cooking contest, and school health promotion activities. It is hypothesized that ultra-Orthodox Jewish Hasidic women exposed to this community intervention will have improved healthy eating behaviors, reduced unhealthy eating behaviors, increased engagement in physical activity and sleep, and reduced risk for obesity (weight, BMI).

Interventions

OTHERSocio-ecologial, community-based intervention

Intervention components will include a health newsletter, health workshops, community evening/health project registration, lay leader training, neighborhood exercise groups, community walking programs with pedometers, healthy cooking contest, and school health promotion activities.

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

This is a quasi-experimental, pre-post study.

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Hebrew, English, or Yiddish speaker * Ultra-Orthodox Jewish Hasidic woman in the targeted community

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Eating behaviorsOne year following project completion (4 years later)Eating behaviors will be assesses through self report of specific food item consumption via questionnaire
Engagement in physical activityOne year following project completion (4 years later)Engagement in physical activity will be assesses through self report of minutes engaged in vigorous and moderate physical activity via questionnaire as well as pedometer step count where relevant
Reduced risk for obesity (weight, BMI).One year following project completion (4 years later)Self report of BMI
Hours of sleepOne year following project completion (4 years later)Hours of sleep will be assesses through self report of average hours slept via questionnaire

Secondary

MeasureTime frameDescription
Stages of Change for targeted health behaviorsOne year following project completion (4 years later)Stages of Change for targeted health behaviors will be assesses through self report questionnaire
Spiritual Health Locus of ControlOne year following project completion (4 years later)Spiritual Health Locus of Control will be measured through Holt's Spiritual Health Locus of Control scale, culturally adapted to the population
health parameters of local population3 years prior to intervention, 2 years after intervention.data will be retrieved from local health plans including lipid profile, weight and hemoglobin a1c
self perceived health statusOne year following project completion (4 years later)self perceived health status will be assessed through self report questionnaire
General Health Self EfficacyOne year following project completion (4 years later)General Health Self Efficacy will be assessed via Ralph Schwarzer's General Health Self Efficacy self report scale, culturally adapted to the population
Cardiovascular disease knowledgeOne year following project completion (4 years later)Cardiovascular disease knowledge will be assesses through self report questionnaire based on the American Heart Association's knowledge survey items

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026