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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00877240
Other study ID # 735-2008
Secondary ID
Status Withdrawn
Phase N/A
First received April 6, 2009
Last updated March 15, 2016
Start date August 2008
Est. completion date August 2009

Study information

Verified date March 2016
Source Medical Corps, Israel Defense Force
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

The goal of this study is to determine the effectiveness of a general intervention that includes encouragement of physical activity and healthy living habits of officers and permanent staff in the IDF


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 26 Years to 55 Years
Eligibility Inclusion Criteria:

- IDF'S staff member

- Age >26

- One or more risk factor

Exclusion Criteria:

- Cardio vascular condition

- Respiratory disease

- Other healthy conditions according to the physician's decision

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Intervention

Behavioral:
Behavioral intervention-to determine the effectiveness of a general intervention on healthy living habits of IDF staff
the program consists of 3 times a week of physical activity, nutrition advice, weight lodd program, stress workshop and smoking cessation workshop

Locations

Country Name City State
Israel IDF's Medical Corps Tel Hashomer

Sponsors (1)

Lead Sponsor Collaborator
Medical Corps, Israel Defense Force

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary physical fitness habits weight reduction balanced nutrition one year No
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