Promoting Health by Self Experience (PHASE) Randomized Controlled Trial
NCT ID: NCT01129895
Last Updated: 2010-06-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
650 participants
INTERVENTIONAL
2010-04-30
2011-05-31
Brief Summary
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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.
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Health promotion
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.
Health promotion
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.
Promoting Health
No intervention follow-up only
No interventions assigned to this group
Interventions
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Health promotion
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.
Eligibility Criteria
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Inclusion Criteria
* Patients age 21-50 in selected clinics
Exclusion Criteria
* Health providers from clinics not in the area of the study
21 Years
50 Years
ALL
No
Sponsors
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Unilever Israel
INDUSTRY
Responsible Party
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Ben-Gurion University
Principal Investigators
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Iris Shai, PhD
Role: PRINCIPAL_INVESTIGATOR
Ben-Gurion University of the Negev
Danit R Shahar, PhD
Role: PRINCIPAL_INVESTIGATOR
Ben-Gurion University of the Negev
Locations
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Clalit Health Services
Petah Tikva, Israel, Israel
Countries
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Facility Contacts
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References
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Shai I, Erlich D, Cohen AD, Urbach M, Yosef N, Levy O, Shahar DR. The effect of personal lifestyle intervention among health care providers on their patients and clinics; the Promoting Health by Self Experience (PHASE) randomized controlled intervention trial. Prev Med. 2012 Oct;55(4):285-291. doi: 10.1016/j.ypmed.2012.08.001. Epub 2012 Aug 12.
Other Identifiers
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unilever-0410-OL
Identifier Type: -
Identifier Source: org_study_id
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