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Clinical Trials/NCT07668544
NCT07668544Not yet recruitingNot Applicable

The Effect of Kinesiophobia Level on Functional Outcomes in Surgically Performed Hand Injuries

Ebru Aloğlu Çiftçi0 sites100 target enrollmentStarted: June 19, 2026Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100

Study Overview

Brief Summary

Hand and forearm injuries are among the most common traumatic injuries and may result in substantial functional limitations, reduced work capacity, and decreased quality of life. Despite advances in surgical repair techniques, recovery outcomes vary considerably among individuals with similar injury characteristics. Psychological factors, particularly fear of movement or reinjury (kinesiophobia), may influence rehabilitation participation and functional recovery after injury.

The aim of this prospective observational study is to investigate the relationship between early kinesiophobia levels and functional outcomes in adults who undergo surgical treatment for traumatic hand or forearm lacerations. Kinesiophobia will be assessed during the acute post-injury period (within 1-5 days after injury) using the Tampa Scale of Kinesiophobia. Injury severity will be evaluated using the Modified Hand Injury Severity Classification (MHISC/MEYCS).

Participants will be followed for 12 weeks after injury. Functional recovery will be assessed at the 8th week using the Buck-Gramcko Score and the Sollerman Hand Function Test, and at the 12th week using the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire and hand grip strength measurements.

The study will examine whether higher levels of early kinesiophobia are associated with greater injury severity and poorer functional recovery. Findings from this study may help identify patients at risk for delayed recovery and support the development of early rehabilitation strategies targeting psychological as well as physical aspects of hand injury recovery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Investigators

Sponsor
Ebru Aloğlu Çiftçi
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Ebru Aloğlu Çiftçi

Lecturer

Istinye University

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