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Recruiting NCT07358507

EFFECTS OF NERVE GLIDING EXERCISES ON ULNAR-SIDED WRIST PAIN

No phase Interventional Ulnar Wrist Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ulnar Nerve Gliding Exercises, Conventional Physiotherapy.
Who it may be relevant to
Registry conditions: Ulnar Wrist Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Investigation of the Effects of Nerve Gliding Exercises on Pain, Function, Joint Position Sense and Weight-Bearing Tolerance in Patients With Ulnar-Sided Wrist Pain

Overview

The purpose of this study is to learn if adding specific "nerve gliding" exercises to a standard physical therapy program helps reduce pain and improve hand function in people with ulnar-sided (pinky side) wrist pain. Participants who have had wrist pain for at least 3 months will be randomly assigned to one of two groups. Both groups will receive a standard treatment program that includes patient education, activity modification, massage, and ice application. One group will also perform specific nerve gliding exercises for the ulnar nerve. Researchers will evaulate pain level, hand function, strength, weight-bearing tolerance, and joint position sense at the beginning and after 4 weeks of treatment to see if the exercises provide extra benefit. The study treatment period lasts for 4 weeks.

Interventions

  • Other Ulnar Nerve Gliding Exercises
    Ulnar nerve gliding exercises will be performed twice a week in the clinic for 4 weeks. Participants will also perform these exercises as a home program 3 times daily.
  • Other Conventional Physiotherapy
    Includes patient education, activity modification, classic massage along the ulnar nerve trace, and ice application (10-12 minutes) at the end of each session.

Primary outcome measures

  • Pain Level [Time frame: From enrollment to the end of treatment at 4 weeks]
Secondary outcome measures (5)
  • Wrist Function [Time frame: Baseline and 4 weeks.]
  • Grip Strength [Time frame: Baseline and 4 weeks]
  • Wrist Strength [Time frame: Baseline and 4 weeks]
  • Weight Bearing Tolerance [Time frame: Baseline and 4 weeks]
  • Joint Position Sense [Time frame: Baseline and 4 weeks.]

Eligibility criteria

Inclusion criteria

  • Being over 18 years of age.
  • History of ulnar-sided wrist pain lasting for at least 3 months.
  • Diagnosis of ulnar-sided wrist pain confirmed by a hand surgeon, which may include: fractures or dislocations of the 4th and 5th metacarpals, hamate, triquetrum, lunate, pisiform, distal ulna, or distal radius; Lunotriquetral ligament tears; Kienböck's disease; Ulnar impaction syndrome; Triangular Fibrocartilage Complex (TFCC) injury; carpal instabilities; DRUJ instability; pisotriquetral arthritis; DRUJ arthritis; extensor carpi ulnaris (ECU) tendon subluxation; or tendinitis of the ECU, extensor digiti minimi, and flexor carpi ulnaris.
  • Adequate cognitive level (scoring 22 or above on the Montreal Cognitive Assessment scale).

Exclusion criteria

  • Presence of other diseases involving the hand and wrist (e.g., carpal tunnel syndrome, Dupuytren's disease).
  • History of traumatic injury to the hand, wrist, and/or forearm within the last 3 months.
  • History of surgery on the hand, wrist, and/or forearm within the last 6 months.
  • Currently receiving treatment for hand and wrist problems.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Gazi University Health Sciences Faculty Physiotherapy and Rehabilitation Department — Ankara

Identifiers

NCT: NCT07358507 · 2025-1761

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗