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Results of Cervical Segmental Mobilization in Patients With Chronic Lateral Epicondylitis

Unknown statusNot applicableNCT06440928
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The aim of our study was to investigate the effect of cervical segmental mobilization on pain, functionality, grip strength and quality of life in patients with chronic lateral epicondylitis. It was planned as a randomized controlled experimental study.

Study details

Official title
Investigation of the Effect of Cervical Segmental Mobilization on Pain, Functionality, Grip Strength and Quality of Life in Patients With Chronic Lateral Epicondylitis
Conditions
  • Epicondylitis of the Elbow
  • Servical Segmental Mobilization
Interventions
  • Behavioral: mobilization
  • Other: standard treatment
  • Other: deep friction
Sponsor
Halic University
Start date
2024-05-15
Primary completion
2024-08-15
Sex
All
Age range
from 25 Years to 44 Years
Results posted
No results posted in this snapshot
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Being between the ages of 25-44 * Being diagnosed with LE by a physician * Not having any defined pathology in the cervical region * No neurological problems in the upper extremities * No history of cervical surgery Exclusion Criteria: * Those with a history of infection, tumor, trauma in the cervical area * Fibromyalgia patients * Congenital or acquired deformities of the upper extremity * History of shoulder or elbow surgery or dislocation * Cervical radiculopathy * Having had Wiplash

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06440928