Evaluation of a Health Promoting Community Center Network (HPCCN) Innovation. (HPCCN)

November 24, 2021 updated by: Donna R Zwas, Hadassah Medical Organization

Evaluation of a Health Promoting Community Center Network (HPCCN) Innovation

The purpose of this research study is to design, implement and evaluate the setting for a "Healthy Community Center". This is a program review of a program which will be planned in a community based participatory level, based on the socioecological model. A pre-post design will be utilized where all community centers in the study will be exposed to the intervention components. It is hypothesized that community centers who will receive the intervention will have better skills at building sustainable participatory effective health promotion projects and will provide a healthy setting for the community within its juristiction.

Study Overview

Detailed Description

The purpose of this research study is to design, implement and evaluate the setting for a "Healthy Community Center". This is a program review of a program which will be planned in a community based participatory level, based on the socioecological model. A pre-post design will be utilized where all community centers in the study will be exposed to the intervention components. All community centers (n=15) will be evaluated by pre intervention questionairres and focus groups of community center Managers and health promotion professionals. The network will be designed upon the foundation of the "Healthy Cities network" with adaptations made in the process of participatory planning and designing according to the results of the focus groups. Intervention will include a a 12 week training session for designated "Health Coordinator" from each community center, Planning and implementing a personolized Health promtion Project in each community centre .It is hypothesized that community centers who will receive the intervention will have better skills at building sustainable participatory effective health promotion projects and will provide a healthy setting for the community within its juristiction.

Study Type

Interventional

Enrollment (Actual)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Jerusalem, Israel, 91120
        • Hadassah Medical Organization

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • People who live within the geographical area of the community centers

Exclusion Criteria:

  • Children under the age of 6 People who do not reside within the geographical area of the community centers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: participating community centers
Training course for the community center health coordinators Professional guidance for the CC health coordinators

These community centers who have volunteered to join the project will receive a 12 week training session which includes the values and principles of health promotion and the principles of building a health promotion project.

The participants will be requested to build a health promotion project within their community. Building and implementing the project will be assisted by a health promotion specialist. Each health promotion project will be evaluated according to the principles of health promotion.

Other Names:
  • Professional guidance for the CC health coordinators

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
project planning, implementation and assessment
Time Frame: 3 years
RE-AIM assessment of Reach, Effectiveness, Adoption, Implementation and Maintenance of the Community Center Programs, assessed by interview, There are 4-6 tailored questions in each domain and the answers are coded as yes, partially and no. Scores range from 0 -93
3 years
Israeli Healthy Cities Network adapted measure
Time Frame: 12 months after intervention initiation
Israeli Healthy Cities Network evaluation tool was designed based on the MARI's (Monitoring Accountability Reporting Impact assessment) framework. It assesses six dimensions of the principles and strategies of the Healthy Cities work: (i) Equity policy and political support. (ii) Management. (iii) Health promotion programs and activities in the city. (iv) Community participation. (v) Intersectoral partnerships (vi) Environmental protection activities. This questionnaire was adapted to a community center framework.
12 months after intervention initiation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
European Quality Instrument for Health Promotion
Time Frame: 6 months after intervention initiation
information on four domains using in-person interviews: (i) compliance with international principles of Health promotion programs, (ii) development and implementation, (iii) project management and (iv) sustainability of programs. each item of the EQUIHP tool was recoded on a scale of 0-1: a score of 0 if the criteria was identified as not fulfilled, 0.5 if partly fulfilled and 1 if fully fulfilled. The sum of all valid scores per programme was divided by the number of valid answers to give the mean score. A mean score was given for each of the four domains, and for the overall score in the same manner. Higher scores are better.
6 months after intervention initiation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 11, 2017

Primary Completion (Actual)

January 1, 2021

Study Completion (Actual)

November 24, 2021

Study Registration Dates

First Submitted

March 1, 2020

First Submitted That Met QC Criteria

July 12, 2020

First Posted (Actual)

July 14, 2020

Study Record Updates

Last Update Posted (Actual)

November 26, 2021

Last Update Submitted That Met QC Criteria

November 24, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • ccproject-HMO-CTIL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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