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A safety net for the toughest transition: can a care team bridge the gap to adult medicine?

NCT ID NCT06093386

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time

Summary

This trial tests whether a dedicated transition team—including a nurse practitioner, a registered nurse, and a social worker—can improve the move from pediatric to adult care for youth with medical complexity. Participants receive two years of intensive support with care planning, funding, and connections to adult providers, compared with usual care. The study asks if this support improves continuity of care, satisfaction, and quality of life.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Intensive transition support from a team of nurses and a social worker
What this could lead to
If successful, this could establish a model for smoother, more supportive transitions to adult care, potentially improving health outcomes and quality of life for youth with complex medical needs.
What could go wrong
The trial is relatively small and focuses on a specific population in Ontario, so results may not apply broadly. The support is intensive and may not be feasible in 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

144 people

The number who actually took part.

Started

Nov 2023

Finished

Apr 2026

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

210 to 213 months

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: * Patients 17 years 6 months- 17 years 9 months old (inclusive) who meet Ontario's CMC definition: 1. technology dependence and/or users of high-intensity care, 2. fragility (severe and/or life-threatening condition, 3. chronicity (expected to last at least 6 months), 4. complexity (involvement of ≥5 healthcare practitioners/teams and healthcare services in ≥ 3 locations such as home, school, hospital, etc.). Exclusion Criteria: * are expected to die within 2 years of recruitment (e.g., those receiving active end-of-life care) * do not have a stable primary caregiver (e.g., those who reside in residential or long-term care facilities, and those in foster care as the intervention is focused on a patient-caregiver dyad)

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • The Hospital for Sick Children

    Toronto, Ontario, Canada