Behavioral Interventions as Primary Prevention for Non-Communicable Diseases Among Young People
1 other identifier
interventional
2,000
1 country
1
Brief Summary
In consistence of North Africa vision to decrease incidence of NCDs in different population type investigators decide to give more concerns to youth (young old) who are the main human power to build future. Recent data report non-communicable diseases (NCDs) are the current leading cause of mortality in Egypt, with NCDs estimated to account for 85% of all deaths. Egypt's youth population (16-25 years old) is both the country's greatest asset and one of its biggest challenges. This age group makes up a huge share of the population, and while they are more connected to technology, social media, and modern facilities than older generations, they face lifestyle barriers that affect their health and productivity. Many modifiable risk factors affect their behavior and in consequence health. These factors related strongly to their close relationship with technology, they spend more time on mobile and computer applications that affect directly on physical inactivity, sleeping time (onset and duration) and at the end cause NCDs as obesity and CVs problems. Upper Egypt as apart from North Africa region is considered as one of the low-income countries with special cultures, specifically regarding food and physical activities. Even though young people constitute a significant proportion of the population, comparatively fewer studies have examined the prevalence of health concerns and the strategies needed to promote their well-being, especially when contrasted with research focused on groups such as the elderly or pregnant and lactating women. This project aims to investigate prevalence patterns, identify contributing factors, enhance community awareness by encouraging training of healthcare providers to best act and modify youth risk factors, and implement preventive interventions that are both cost-effective and sustainable. Furthermore, it seeks to foster adherence to these measures to strengthen health literacy and reduce the burden of conditions
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 30, 2026
CompletedStudy Start
First participant enrolled
April 1, 2026
CompletedFirst Posted
Study publicly available on registry
April 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2028
April 17, 2026
April 1, 2026
1 year
March 30, 2026
April 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
BMI control
Measurements of BMI, before weigh/length square after 6 months and 1 year from following in the program
6-12 months
Secondary Outcomes (2)
Blood pressure contrl
6-12 months
Blood glucose levels
6_12 months
Other Outcomes (1)
Smoking cessation
6-12 months
Study Arms (2)
behavior therapy
EXPERIMENTALControl group
NO INTERVENTIONNormal life style
Interventions
User Experience (UX) / User Interface (UI) design followed by rapid prototyping. Integration of Behavioral Change Techniques (BCTs) like nudging, peer-to-peer rewards, and goal setting
Eligibility Criteria
You may qualify if:
- Age Range: Typically 10-19 (adolescents) or 15-24 (young adults).
- resident in Egypt
- accept sharing and adhered for following
- At-risk youth (e.g., sedentary, high-sugar diet)
- Motivated to use digital tools
- Diverse socio-economic backgrounds
- Healthy enough for moderate exercise
- Presence of at least one modifiable risk factor, such as:
- Insufficient physical activity (not meeting WHO guidelines of 60 min/day). Unhealthy dietary habits (high sugar/salt intake, low fruit/vegetable consumption).
- Tobacco use or exposure to second-hand smoke (including vaping). Harmful alcohol consumption patterns.
You may not qualify if:
- Individuals already diagnosed with the NCDs being targeted
- Presence of medical conditions that cause secondary obesity or hypertension
- Current use of medications that significantly affect metabolic or behavioral outcomes
- Individuals with active psychosis, severe clinical depression, or eating disorders
- Severe impairments that prevent the individual from understanding the study requirements, providing informed assent, or interacting with digital intervention tools
- Enrollment in another clinical trial or behavioral intervention that might lead to "treatment contamination."
- Unable to consent or use tech due to severe deficit
- Temporary residents (will move before data collection ends)
- Safety risk (e.g., severe heart condition)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Deraya university
Minya, 05673, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 30, 2026
First Posted
April 14, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
January 1, 2028
Last Updated
April 17, 2026
Record last verified: 2026-04