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Clinical Trials/NCT01129895
NCT01129895UnknownNot Applicable

Promoting Health by Self Experience (PHASE) Randomized Controlled Trial

Unilever Israel1 site in 1 country650 target enrollmentStarted: April 1, 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
650
Locations
1
Primary Endpoint
Promoting Health randomized controlled trial

Study Overview

Brief Summary

Promoting Health by Self Experience (PHASE) randomized controlled trial

Study Hypothesis:

A personal experience in health promotion will affect the health prevention activities of the health providers and thus will impact their prevention activities toward their patients compared with a control (no-intervention) group.

Detailed Description

Objective

To evaluate the effectiveness of a personal experience and personal initiation program on the health prevention activities of the health providers and the following impact on their patients compared with a control (no-intervention) group.

Methods: A randomized controlled trial Randomization: Health providers of all disciplines will be recruited from 10 clinics of Clalit Health Services, Dan district and randomized using cluster (by clinic) randomization, into an intervention and a control group. In each clinic 15 health care providers and 50 patients will be interviewed providing a total of 150 health care providers and 500 patients.

Intervention: The intervention will be delivered by psychologists and social workers trained in group facilitation and experimental learning. The program is based on theories of experimental learning and Bridges model of change. In each intervention clinic 5 workshops on the initiation of health prevention projects in each clinic will be organized by the intervention team and than the clinic will be followed by the intervention team for 6 months. No intervention will be provided to the control clinics.

Outcomes: changes in quality measurements of both intervention and non-intervention clinics. Among health providers changes in attitudes, personal views and life style as well as health prevention activities will be assessed by questionnaires. A random sample of 50 patients age 21-50 from each of the participating clinics will be selected and interviewed using a questionnaire. The questionnaires will include questions regarding the administration of screening tests, treatment of abnormal measurements, life style changes and satisfaction with the performance of the clinic and health care providers. The evaluation for both health care providers and patients will be performed at baseline and after 6 months.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
21 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Health providers in selected clinics
  • Patients age 21-50 in selected clinics

Exclusion Criteria

  • Patients age younger than 21 and older than 50
  • Health providers from clinics not in the area of the study

Outcomes

Primary Outcomes

Promoting Health randomized controlled trial

Time Frame: 6 months

Changes in quality measurements Changes in attitudes, personal views and life style as well as health prevention activities

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Unilever Israel
Sponsor Class
Industry

Study Sites (1)

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