Prevention Program- Promoting Self Resilience, Positive Self-Image and Body Image Among Adolescents and Their Parents
NCT ID: NCT03540277
Last Updated: 2022-01-24
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
420 participants
INTERVENTIONAL
2018-11-01
2021-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Adolescents as Change Agents in the Incorporation of a Parental Component for a School Based Prevention Program
NCT04688619
A Prevention Program to Encourage Self-care, Self-esteem and Body-esteem Among Young Adolescents
NCT05103371
Increasing the Impact of a School Prevention Program Among Young Adolescents by Adding a Teacher Component
NCT05102526
Integrated Intervention for Caregivers--Open Trial
NCT03487575
Integrated Intervention for Caregivers--Pilot RCT
NCT03487627
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
"In Favor of Myself" is a preventive intervention program. The program's primary goal is to increase adolescents' self-esteem and to prevent negative self-image and body image, as well as to development media literacy. In this study, the investigators will focus on the "Young In Favor of Myself " program, designed for ages 10-12, grades 5 and 6, and its main core is the development of self-care. To increase the effect of "Young In Favor of Myself " program, on the adolescents, the investigators have developed a program that will be passed on to parents through a telephone application. The study will first assess the parents' influence on the program, and then evaluate the difference in adolescent outcomes from the program with or without this supplement.
Results will be measured using the study questionnaire, to be filled out by the participants (both parents and adolescents) before, after, and three months after the completion of the program. The questionnaire will include validated questionnaires with good psychometric qualities. The study protocol was approved by Tel Hai College institutional review board. Parents of all participants, in the intervention and in the control group, received information about the program and the study and were asked to provide informed consent.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Prevention Program "young In Favor of Myself", active parents
The program "young In Favor of Myself" will be delivered to adolescence aged 10-12, over 3 months. The program contains nine weekly, 90-min sessions that focus on Media literacy, self-esteem, self-image and body image. The parents will also participate by a phone app that will pass the parents activities to do with their children, in parallel to the program. All participants will complete a self-report questionnaire at baseline, after the program ends, and three months after the completion of the program.
Experimental: Prevention Program "young In Favor of Myself", active parents
Prevention program: "young In Favor of Myself", with parent participation
Prevention Program "young In Favor of Myself", passive parents
The program "young In Favor of Myself" will be delivered to adolescence aged 10-12, over 3 months. The program contains nine weekly, 90-min sessions that focus on Media literacy, self-esteem, self-image and body image. The parents won't participate in the program, they will get only a brochure about Media literacy, self-esteem, self-image and body image. All participants will complete a self-report questionnaire at baseline, after the program ends, and three months after the completion of the program.
Experimental: Prevention Program "young In Favor of Myself", no parental involvement
Prevention program: "young In Favor of Myself", without parent participation
control group
The control group will not receive the intervention program. The control group will complete the same self-report questionnaire as the intervention group at baseline, after the program ends, and three months after the completion of the program.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Experimental: Prevention Program "young In Favor of Myself", active parents
Prevention program: "young In Favor of Myself", with parent participation
Experimental: Prevention Program "young In Favor of Myself", no parental involvement
Prevention program: "young In Favor of Myself", without parent participation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 10-12-year-old children of participating parents
* Participants who filled out the questionnaires before and after the program
* Participants whose parents signed a letter of informed consent.
Exclusion Criteria
10 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Tel Hai College
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Moria Golan, Prof.
Role: PRINCIPAL_INVESTIGATOR
Tel Hai College
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Tel Hai Academic College
Kiryat Shmona, North of Israel, Israel
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Golan M, Benifla S, Samo A, Alon N, Mozeikov M. Feasibility and effect of adding a concurrent parental component to a school-based wellness program using two modes of mobile-based technology - mixed methods evaluation of RCT. BMC Public Health. 2022 Feb 14;22(1):297. doi: 10.1186/s12889-022-12581-7.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Tel Hai College.
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.