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New program aims to smooth tough transition for teens with eating disorders

NCT ID NCT07518641

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Mar 2028

An estimate. End dates often move.

Lead sponsor

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

16 years and older

Sex

Anyone

Healthy volunteers

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

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.

eating disorder Feeding and Eating Disorders

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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • McMaster University

    Hamilton, Ontario, L8N3Z5, Canada

  • University of Calgary

    Calgary, Alberta, T2N 1N4, Canada

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