Actively Recruiting

Phase Not Applicable
Age: 16Years - 21Years
All Genders
Healthy Volunteers
NCT07145671

The COCCOS Study: a Transition Program for Young Persons With Chronic Conditions

Led by Universiteit Antwerpen · Updated on 2025-08-28

150

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

U

Universiteit Antwerpen

Lead Sponsor

U

University Ghent

Collaborating Sponsor

AI-Summary

What this Trial Is About

A study is undertaken to examine the feasibility of the newly developed transition program in adolescents with type 1 diabetes, asthma and obesity in a multicentric setting. Specific objectives for this study are: (1) examining the impact of the program in terms of patient-reported health outcomes, (2) examining patients' and healthcare providers' experiences related to the program implementation process, and (3) examining the impact of the program in terms of cost-effectiveness.

CONDITIONS

Official Title

The COCCOS Study: a Transition Program for Young Persons With Chronic Conditions

Who Can Participate

Age: 16Years - 21Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • For intervention group participants: 17 years old
  • Diagnosed with type 1 diabetes, asthma, and/or obesity
  • Had at least one pediatric outpatient visit in one of the study hospitals within the past 12 months
  • Dutch speaking
  • Planned to transfer to adult care within the next 12 months
  • For control group participants: 17.5 to 18 years old
  • Diagnosed with type 1 diabetes, asthma, and/or obesity
  • Had at least one pediatric outpatient visit in one of the study hospitals within the past 12 months
  • Dutch speaking
  • Planned to transfer to adult care within the next 12 months
Not Eligible

You will not qualify if you...

  • Patients with severe mental, cognitive, or neurological problems

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ghent University Hospital

Ghent, Belgium, 9000

Actively Recruiting

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Research Team

E

Eva Goossens, Professor

CONTACT

N

Natwarin Janssens

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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