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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04138732
Other study ID # 723HBM- HMO-CTIL
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 15, 2016
Est. completion date December 31, 2020

Study information

Verified date June 2022
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to characterize the existing health behaviors and obstacles to healthy lifestyle among the medical staff in a maternity ward in order to develop a specifically-tailored intervention to help improve the health behaviors of hospital shift workers.The findings will be used to establish a community-based participatory health-promoting program in the ward, engaging the staff in its development and implementation.


Description:

The purpose of this study is to characterize the existing health behaviors and obstacles to healthy lifestyle among the medical staff in a maternity ward in order to develop a specifically-tailored intervention to help improve the health behaviors of hospital shift workers. Shift-work has been associated with unhealthy lifestyles and increased risk of digestive disorders, heart conditions, various kinds of cancer, reproductive dysfunction, and mental conditions. Thus, the findings will be used to establish a community-based participatory health-promoting program in the ward, engaging the staff in its development and implementation. Community Based Participatory (CBP) approach will be used to build an evaluation and intervention. Baseline/needs assessment will be performed by mixed methods approach, combining in depth interviews with key personnel, focus groups and questionnaires that ask about demographics, physical activity and nutrition behaviors, stress, burnout, BMI, and cardiac risk factors.


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Doctors, nurses, secretaries, and assistants Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Improve health behaviors of medical personel
This arm will receive the intervention treatment aimed to help improve their health behaviors, as determined by employee-based steering committee. Interventions will target nutrition, physical activity and stress reduction

Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiac risk factors Initially assessed by in depth interviews with key personnel and focus groups and then assessed by self report through questionnaires. at the end of the 1 year treatment
Secondary BMI pre and post assesment of BMI via self reporting at the end of 1 year of treatment
Secondary Burnout Initially assessed by in depth interviews with key personnel and focus groups and then assessed by self report through questionnaires. at the end of the 1 year treatment,
Secondary Nutrition behaviors Initially assessed by in depth interviews with key personnel and focus groups and then assessed by self report through questionnaires assessing mediterrean diet adherence and western diet behavior at the end of the 1 year treatment
Secondary Physical activity minutes per week Initially assessed by in depth interviews with key personnel and focus groups and then assessed by self report through questionnaires. at the end of the 1 year treatment
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