- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06622681
Integrative Adolescence Research Programme (IARP) (IARP)
December 22, 2025 updated by: Johan Eriksson, Institute for Human Development and Potential (IHDP), Singapore
Integrative Adolescence Research Programme (IARP) - iAdoRe Study
This study aims to understand child health during adolescence.
We will examine the role of lifestyle (e.g.
physical activity), growth trajectories and other environmental factors that can influence the development of phenotypes in adolescence which confer risk for later physical and mental disorders.
With this study, we will develop a deeper understanding of adolescent health and well-being and their main determinants in the local Singaporean context, identify levers for early interventions to mitigate challenges to adolescent health and well-being and enhance protective factors for adolescents to do well in life, contribute to society and maximize their potential.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
The study aims to advance current public policy and health service practices by developing public health, clinical and commercially valuable interventions within the context of expanding commercial partnerships and building multidisciplinary translational research capacity in Singapore.
In addition to the early life period (i.e., the first 1,000 days), the adolescent period has been identified as a crucial second window of opportunity to influence human development and improve life-long well-being.
Adolescence is a key developmental period for body, brain and socioemotional changes.
Puberty is characterised by growth spurts and sexual maturation.
Concurrently, the brain undergoes maturation processes that underlie higher cognitive functions.
The combination of biological changes and environmental influences affect adolescent socioemotional and behaviour patterns.
There is a need to raise the human potential of adolescents who will go on to become the next generation of our adult workforce, so that they lead productive, healthy, and fulfilling lives.
Yet, in many developed countries, the rates of loss of subjective well-being in young people have at least doubled in the decade prior to COVID-19 and have continued to rise since 10.
In the Singapore Youth Epidemiology and Resilience Study (2020-2022), 1 in 3 youths reported experiencing mental health symptoms 11.
This requires the development of a cohesive response system designed to deal with the numerous factors influencing adolescent physical and mental health.
Moreover, it is essential to investigate the developmental origins of metabolic diseases and neurodevelopmental disorders, which both form a major public health burden in Singapore, from as early as the adolescence phase.
A transdisciplinary approach is essential to help adolescents directly recognise their diverse concerns, challenges and experiences and better understand how to manage their health and well-being.
This requires going beyond traditional psychological models of mental health to examine the influences of brain and body interaction, socio-affective, behavioural and psychological development that shape adolescents' well-being.
At present, there is no comprehensive multi-disciplinary (brain-body-environment) study in the general population which examine adolescent health and well-being holistically in Asia.
Findings from primarily Western countries cannot be easily extrapolated to the Singaporean/Asian setting.
A new holistic programme will be essential to advance the health of Asian adolescents.
Study Type
Observational
Enrollment (Estimated)
1200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Janet Lim
- Phone Number: 88546302
- Email: janet_lim@sics.a-star.edu.sg
Study Locations
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-
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Singapore, Singapore
- Enrolling by invitation
- Singapore Institute of Clinical Sciences
-
-
Singapore
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Singapore, Singapore, Singapore, 117609
- Recruiting
- A*STAR Institute for Human Development and Potential (IHDP)
-
Contact:
- Janet Lim, BS
- Phone Number: 6407 0364
- Email: janet_lim@sics.a-star.edu.sg
-
-
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
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Secondary students aged between 13 -15 years old, studying in MOE registered schools in Singapore.
Part of the DREAMS study cohort.
Description
Inclusion Criteria:
- Aged 13 to 15 years of age
- Currently studying in MOE registered school
- Part of the DREAMS study
Exclusion Criteria:
- Not in MOE registered school
- Not part of the DREAMS 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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Participant of the study
Adolescents at 13- 15 years of age, currently studying in MOE-registered secondary school in Singapore and part of the DREAMS cohort.
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child health and environmental factors
Time Frame: 2 years
|
Child's physical health and environment status
|
2 years
|
|
Social Science factors
Time Frame: 2 years
|
Child's mental health status
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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)
May 21, 2024
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
September 30, 2024
First Submitted That Met QC Criteria
September 30, 2024
First Posted (Actual)
October 2, 2024
Study Record Updates
Last Update Posted (Actual)
December 30, 2025
Last Update Submitted That Met QC Criteria
December 22, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 2024-1200
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
PDPA of study participants who are minors
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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