New program aims to smooth tough transition for teens with eating disorders
NCT ID NCT07518641
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a structured program called TransitionED designed to help youth aged 16+ with eating disorders move from pediatric to adult healthcare. The program includes planning packages, guided meetings, and a personal profile to share with new providers. Researchers will check if the program is practical and acceptable in real hospital settings, involving 60 youth, their caregivers, and clinicians.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TransitionED Healthcare Transition Framework (behavioural intervention)
- What this could lead to
- If successful, this could provide a practical, evidence-based model to improve care transitions for youth with eating disorders, reducing gaps in treatment.
- What could go wrong
- This is a small feasibility study (60 participants) with no control group, so it cannot prove the program improves health outcomes. Results may not apply to all settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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16 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Youth and Young Adults (YYA): * Currently receiving paediatric eating disorder care at a participating study site. * Age 16 years or or older (approaching age-based transition to adult-care) * Expressed interest in transitioning to adult eating disorder care or other appropriate adult mental health services * Identified by the clinical team as appropriate to begin formal transition planning (e.g., sufficient transition readiness and interest in ongoing care) * Able and willing to provide informed consent/assent (as applicable at the site) and participate in study procedures Caregivers: * One caregiver (e.g., parent/legal guardian) of a participating YYA * Able and willing to provide informed consent and participate in study procedures (including questionnaires and interviews) Clinicians (intervention deliverers): * Patient facing clinician at a participating site who provides transition support for participating YYA/caregivers and is responsible for delivering intervention components (e.g., joint meeting(s), communication/coordination related to the transition). * Able and willing to provide informed consent and participate in study procedures (e.g., focus groups) Implementation Team Members: * Program leadership/managers/senior clinicians at a participating site involved in implementation of the intervention at that site. * Able and willing to provide informed consent and participate in study procedures (e.g., focus group). Exclusion Criteria: YYA: * Not receiving pediatric eating disorder care at a participating site. * Under age 16 years * Does not express interest in transitioning to adult eating disorder care or other appropriate adult mental health services. * Not identified by the clinical team as ready/appropriate to engage in formal transition planning during the study period (e.g., insufficient transition readiness or not currently at the transition-planning stage). * Unable to provide informed consent/assent or unable to participate in study procedures (e.g., due to significant cognitive/communication barriers as determined by the clinical/research team). Caregivers: * Not the caregiver of an enrolled YYA (only one caregiver per YYA is enrolled). * Unable to provide informed consent or participate in study procedures. Clinicians and Implementation Team Members: * Not affiliated with a participating site or not in an eligible role as defined above. * Peripheral providers who may be involved in care but are not enrolled as participants (e.g., family physicians or adult providers who might attend a joint meeting). * Unable to provide informed consent or participate in study procedures.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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McMaster University
Hamilton, Ontario, L8N3Z5, Canada
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University of Calgary
Calgary, Alberta, T2N 1N4, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Smarter scoring could slash hospital return rates
- New integrated therapy approach aims to transform eating disorder care
- Hidden danger: eating disorders worsen blood sugar in type 1 diabetes
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