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New hand therapy combo aims to boost wrist healing after fracture

NCT ID NCT07288060

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Sep 04, 2026 · Updated 1 time

Summary

This study tests two additional therapies for people recovering from a broken wrist (distal radius fracture) treated with surgery. One therapy uses gentle manual movements (Mulligan mobilisation), and the other uses mental imagery exercises (graded motor imagery) to retrain the brain. Both are added to standard physical therapy. The goal is to see if they improve joint position sense, reduce fear of movement, and enhance function. The study will include 33 adults aged 25–65 and follow them for 6 weeks.

What this could mean

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

Active substance
Mulligan mobilisation and graded motor imagery therapy
What this could lead to
If successful, these therapies could improve joint awareness and reduce fear of movement after wrist fracture, leading to better recovery.
What could go wrong
This is a small, early-phase study with only 33 participants, so results may not apply widely. The treatments are add-ons to standard rehab, so any benefit may be modest.

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

39 people

The number who actually took part.

Started

Nov 2025

Finished

Aug 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

25 to 65 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: * Age between 25 and 65 years * Clinical diagnosis of distal radius fracture * Indicated for surgical treatment * Surgical fixation performed using plate and screw technique * Willing and able to provide informed consent and participate in the study Exclusion Criteria: * Inability to read or write * Presence of additional orthopedic, neurological, or cardiovascular disorders * History of surgery involving the ipsilateral upper extremity within the past 6 months * Visual or hearing impairment that would interfere with adherence to treatment or study assessments

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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.

Contacts and locations

Locations

  • Istanbul Aydın University

    Istanbul, Turkey (Türkiye)

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