Fear of Re-Injury may slow hand recovery after surgery
NCT ID NCT07668544
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 100 adults who had surgery for hand or forearm injuries to see if fear of movement (kinesiophobia) affects how well they recover. Participants fill out questionnaires and take hand function tests over 12 weeks. The goal is to understand if early fear levels can predict who might have a harder time healing, so doctors can offer better support.
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 this study finds a link between fear of movement and poor recovery, it could lead to new rehab programs that address both mental and physical aspects of hand injury healing.
- What could go wrong
- This is an observational study, not a treatment trial. It only looks for associations, so it cannot prove that fear causes worse outcomes. The results may not apply to all hand injuries.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
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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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: Adults aged 18 years and older. Patients presenting to the emergency department with traumatic hand or forearm lacerations requiring surgical treatment. Injury involving one or more anatomical structures of the hand or forearm (skin, tendon, nerve, vessel, or combined injuries). Assessment within 1-5 days following injury. Ability to understand and complete study questionnaires and functional assessments. Provision of written informed consent. Willingness to participate in follow-up assessments at 8 and 12 weeks after injury. Exclusion Criteria: Age younger than 18 years. Cognitive impairment, severe psychiatric disorder, or communication problems preventing completion of questionnaires. Previous major injury, surgery, or permanent functional impairment of the affected upper extremity. Polytrauma or additional injuries that may substantially affect upper extremity function or rehabilitation outcomes. Neurological disorders affecting upper extremity function (e.g., stroke, peripheral neuropathy, spinal cord injury). Severe musculoskeletal disorders of the upper extremity unrelated to the index injury. Inability or unwillingness to attend follow-up evaluations. Refusal to provide informed consent
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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 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.
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