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RecruitingNCT07291505Updated Mar 10, 2026

The Investigation of Kinesiophobia in Conservative Distal Radius Fractures

An observational study in Distal Radius Fracture, Kinesiophobia and Functional Status, sponsored by Pamukkale University. Recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-03-10.

Sponsored by Pamukkale University · Observational

From the registry’s dates

  • Started Feb 2026; still recruiting 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
34
Ages
18 Years to 65 Years
Sex
All
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Study summary

This study aimed to investigate the predictability of kinesiophobia on functional outcomes in conservatively treated patients with distal radius fractures. For this purpose, patients' level of kinesiophobia will be assessed using the Tampa Kinesiophobia Scale. To assess the functional status of patients, joint range of motion and upper extremity weight bearing measurements will be performed. Patients' functionality will be additionally assessed with the Patient Rated Wrist Evaluation Questionnaire.

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Conditions studied

  • Distal Radius Fracture
  • Kinesiophobia
  • Functional Status

Keywords

  • Tampa Scale of Kinesiophobia
  • distal radius fracture
  • wrist function
  • upper extremity weight bearing
03

In context

Wrist Fractures

330 studies on the registry are indexed under Wrist Fractures; 73 are open to participants now.

This study's planned enrollment of 34 is below the median of 100 across 53 observational studies indexed under Wrist Fractures.

Browse Wrist Fractures studies →

Lead sponsor

Pamukkale University is the lead sponsor of 342 studies on the registry; 61 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Volunteers among the patients who were referred to the hand rehabilitation unit after being followed conservatively with a diagnosis of distal radius fracture in the hand surgery clinic of a university hospital will be included in the study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Having been treated conservatively with an isolated distal radius fracture diagnosis,
  • Having a cognitive level that allows one to understand assessment methods and apply instructions.

Exclusion criteria

Exclusion Criteria:

  • Comorbid musculoskeletal-neurovascular injuries
  • Bilateral injuries
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
34 participants (estimated)
Target follow-up
18 Weeks
Patient registry
Yes

Groups and cohorts

  • Patients treated conservatively with a diagnosis of distal radius fracture

    Other: Questionnaire and Physical Exam

Interventions

  • OtherQuestionnaire and Physical Exam

    A goniometric assessment will be performed to measure the range of motion in the wrist-forearm joint, and a Push Off test will be conducted to measure the upper extremity weight-bearing capacity. Additionally, the Tampa Scale of Kinesiophobia and Patient-Rated Wrist Evaluation Questionnaire will be administered to patients using a face-to-face assessment method.

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What researchers measure

Primary outcomes

  1. Tampa Scale of Kinesiophobia

    It is a 17-item scale scored using a 4-point Likert scale (1 = Strongly disagree, 4 = Strongly agree). A total score is calculated after reversing items 4, 8, 12, and 16. The individual receives a total score between 17 and 68. A high score on the scale indicates a high level of kinesiophobia.

    Time frame: At 12 and 18 weeks after injury

  2. Goniometric measurement

    Patients' forearm pronation and supination, as well as wrist flexion, extension, radial and ulnar deviation movements, will be measured using a universal goniometer.

    Time frame: At 12 and 18 weeks after injury

  3. Push-Off Test

    It determines the force that the person can exert on their injured limb. The measurement will be taken using a Jamar hand dynamometer. While the person is standing, with the shoulder at 30 degrees of extension and the elbow at 30 degrees of flexion, the measurement will be repeated three times and the average recorded in kilograms.

    Time frame: At 12 and 18 weeks after injury

  4. Patient-Rated Wrist Evaluation

    It measures the severity of wrist pain and the level of disability in activities of daily living. The survey consists of two subsections with a total of 15 questions. Each question is answered on a scale of 0 to 10 (0 = no pain/difficulty; 10 = maximum pain felt/inability to perform). The scores for the pain and function sections are added together to determine the final score, which is calculated out of 100. A high score indicates a high level of pain and disability.

    Time frame: At 12 and 18 weeks after injury

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Study locations

1 of 2 sites recruiting
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References and documents

Publications

  • Jayakumar P, Teunis T, Vranceanu AM, Lamb S, Ring D, Gwilym S. Early Psychological and Social Factors Explain the Recovery Trajectory After Distal Radial Fracture. J Bone Joint Surg Am. 2020 May 6;102(9):788-795. doi: 10.2106/JBJS.19.00100. PubMed 32379119 ↗
  • Goudie ST, Broll R, Warwick C, Dixon D, Ring D, McQueen M. The Association Between Psychological Factors and Outcomes After Distal Radius Fracture. J Hand Surg Am. 2022 Feb;47(2):190.e1-190.e10. doi: 10.1016/j.jhsa.2021.04.012. Epub 2021 Jun 8. PubMed 34112544 ↗

Individual participant data

Plan to share: Undecided

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07291505
Responsible party
UMUT ERASLAN (Assistant Professor, Pamukkale University) — Principal investigator
First posted
Dec 18, 2025
Start date
Feb 2, 2026
Primary completion
Dec 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Mar 10, 2026

Study contacts

Umut Eraslan, PhD
Contact
ueraslan@pau.edu.tr
+905444126520

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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