EFFECTS OF NERVE GLIDING EXERCISES ON ULNAR-SIDED WRIST PAIN
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
1 other identifier
interventional
34
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 23, 2025
CompletedFirst Submitted
Initial submission to the registry
January 14, 2026
CompletedFirst Posted
Study publicly available on registry
January 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedJanuary 22, 2026
January 1, 2026
3 months
January 14, 2026
January 14, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Pain Level
Pain level will be evaluated using the Visual Analog Scale (VAS) for pain at rest, during activity, and at night.
From enrollment to the end of treatment at 4 weeks
Secondary Outcomes (5)
Wrist Function
Baseline and 4 weeks.
Grip Strength
Baseline and 4 weeks
Wrist Strength
Baseline and 4 weeks
Weight Bearing Tolerance
Baseline and 4 weeks
Joint Position Sense
Baseline and 4 weeks.
Study Arms (2)
Control Group
ACTIVE COMPARATORParticipants in this group will receive standard treatment consisting of patient education, activity modification, massage, and ice application for 4 weeks.
Mobilization Group
EXPERIMENTALParticipants in this group will receive standard treatment including patient education, activity modification, massage, and ice application. In addition, they will perform ulnar nerve gliding exercises for 4 weeks.
Interventions
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.
Includes patient education, activity modification, classic massage along the ulnar nerve trace, and ice application (10-12 minutes) at the end of each session.
Eligibility Criteria
You may qualify if:
- 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).
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Gazi Universitylead
- Ankara Universitycollaborator
Study Sites (1)
Gazi University Health Sciences Faculty Physiotherapy and Rehabilitation Department
Ankara, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Master's Student
Study Record Dates
First Submitted
January 14, 2026
First Posted
January 22, 2026
Study Start
October 23, 2025
Primary Completion
February 1, 2026
Study Completion
February 1, 2026
Last Updated
January 22, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share