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New study to uncover how tics disrupt sleep in kids with tourette syndrome

NCT ID NCT07450079

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 1 time

Summary

This study will look at sleep in 34 children with Tourette syndrome, comparing them to children without the condition. Researchers will use a special tic index, a watch-like movement tracker, and overnight sleep recordings to see how tics affect sleep quality. The goal is to better understand sleep problems in these children and support future research.

What this could mean

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

What this could lead to
If successful, this study could help researchers better understand how tics affect sleep in children with Tourette syndrome, potentially guiding future treatments for sleep problems.
What could go wrong
This is a small, observational study that is not yet recruiting. It does not test any treatment, so it will not directly improve sleep or tics. Results may not apply to all children with Tourette syndrome.

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.

Participants

About 34 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Sep 2027

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.

Who is studied

Participants will be between the ages of 6-17. All participants will have been referred to the sleep service team, known by the Tics and neuro-developmental movements (TandDEM) team, and will meet the diagnostic criteria for TS according to the International Classification of Diseases (ICD-10; F95.2).

Ages

6 to 17 years

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 already under investigation by Evelina London Children's Hospital for sleep disturbances * Diagnosis of Tourette Syndrome in accordance with the International Classification of Diseases (ICD-10;F95.2) * Ages 6-17 at time of recruitment, and not between transition or due to transition to adult services * Have had a successful and compliant PSG, ideally within 6 months of recruitment * Participants able to understand patient information and can provide informed assent * Participants have parent and/or guardian willing to provide informed consent on behalf of the child Exclusion Criteria: * Any physician diagnosed chronic medical condition that could impact their study participation * Non-verbal participants without access to appropriate communication support * Non-English-speaking participants without access to appropriate translator

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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

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  1. 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 ↗

  2. A doctor treating you

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