- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04136938
Social Marketing in Prevention Actions
July 9, 2024 updated by: Centre Hospitalier Universitaire de Saint Etienne
Impact of Social Marketing in Collective Prevention Actions : Case of Fall Prevention Workshop Among Elderly Living in Three French Departments.
Physical Activity (PA) is recognized as the most effective method to prevent falls in the elderly.
Yet despite there being a consensus now that Physical Activity (PA) is effective in practice, there remain many obstacles to participation and attendance resulting in Physical Activity (PA) approaches designed to prevent falls actually only benefiting a limited number of elderly subjects.
Social marketing has already shown its utility in the construction of prevention programs.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study uses the social marketing approach to improve a fall prevention program. The intervention territory will receive social marketing campaign while the territory controls will not have a campaign.
The main goal is to improve attendance at our fall prevention program.
Study Type
Observational
Enrollment (Actual)
210
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
-
-
-
Saint-etienne, France
- CHU Saint-Etienne
-
-
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
56 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
People aged 60 and over.
Description
Inclusion Criteria:
- People living in the one of the territories of the study
- People without medical contraindications to participate in moderate physical activity
- People who has received information about the study and its rights to its data
Exclusion Criteria:
- People unable to attend workshops
- People already registered for adapted physical activity
- People who refused to participate to the study.
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
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Intervention group (social marketing campaign)
People aged 60 and over will be included.
They will receive a social marketing campaign.
|
A social marketing campaign of prevention workshop sessions will be performed.
|
|
Control group
People aged 60 and over will be included.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of attendance rate of participants at social marketing campaign (%)
Time Frame: Years: 1
|
Comparison rate of attendance rate of participants at prevention workshop sessions (%) between interventional and control group.
|
Years: 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of attendance rate of participants at fall prevention workshop sessions (%)
Time Frame: Years: 1
|
Comparison rate of attendance rate of participants at prevention workshop sessions (%) between interventional and control group.
|
Years: 1
|
|
Life quality of participants measured by SF-36 questionnaire score
Time Frame: Years: 0, 1
|
The SF-36 is a self-questionnaire to assess the quality of life and contains 36 items with minimum score 0 (bad quality life) and maximum score at 100 (good quality life).
|
Years: 0, 1
|
|
Physical activity level of participants measured by IPAQ questionnaire
Time Frame: Years: 0, 1
|
The International Physical Activity Questionnaire (IPAQ): short version for elderly people is a self-questionnaire to assess the Physical Activity and contains 7 items.
Computation of the total score for the short form requires summation of the duration (in minutes) and frequency (days) of walking, moderate-intensity and vigorous-intensity activities.
|
Years: 0, 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Luc GOETHALS, PhD student, Jean Monnet University
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)
March 9, 2020
Primary Completion (Actual)
July 1, 2021
Study Completion (Actual)
July 1, 2021
Study Registration Dates
First Submitted
October 18, 2019
First Submitted That Met QC Criteria
October 21, 2019
First Posted (Actual)
October 23, 2019
Study Record Updates
Last Update Posted (Actual)
July 10, 2024
Last Update Submitted That Met QC Criteria
July 9, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRBN622019/CHUSTE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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