Sedentary Behavior Clinical Trial
Official title:
Womens Leadership Intervention Program
Goal of the Program: To develop personal and group ability for participants in the DPP to plan and implement health promotion programs. Objectives: 1. Develop skills in the planning, implementation, and assessment of community-based health promotion programs 2. Personal, group and community capacity development in health promotion
Status | Recruiting |
Enrollment | 150 |
Est. completion date | December 31, 2025 |
Est. primary completion date | August 31, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 99 Years |
Eligibility | Inclusion Criteria: - had to previously take part in the previously implemented diabetes prevention program (DPP) - had to have interest and ability in developing programs Exclusion Criteria: - |
Country | Name | City | State |
---|---|---|---|
Israel | Hadassah Medical Organization | Jerusalem |
Lead Sponsor | Collaborator |
---|---|
Hadassah Medical Organization | Jerusalem Municipality |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Program implementation | Three programs will be implemented by the group within 12 months of initiation of the course. | 12 months after completion of the course | |
Primary | RE-AIM assessment of intervention quality | The RE-AIM assessment tool assesses Reach, Effectiveness, Adoption, Implementation, and Maintenance of the intervention programs. Each domain is assessed by questions adapted from the RE-AIM framework. Each item is scored as fully implemented, partially implemented or not implemented, with 0 as not, 0.5 as partially and 1.0 as fully, The questions for each item are averaged for a score that ranges from 0-1, with one being full implementation | 12 months after completion of the course | |
Secondary | health promotion leadership self efficacy | 13 item questionnaire with scores ranging from 13- 52, with 52 representing higher self efficacy | upon completion of the course, approximately 14 weeks after initiating the intervention. |
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