Results of Cervical Segmental Mobilization in Patients With Chronic Lateral Epicondylitis

Epicondylitis of the Elbow Clinical Trial

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06440928
• Other study ID #: 2023/106
• Status: Recruiting
• Phase: N/A
• Start date: May 15, 2024
• Est. completion date: October 15, 2024

Study information

• Verified date: May 2024
• Source: Halic University
• Contact: mustafa yigilitas, doctorate
• Phone: 05309782720
• Email: fztmy77[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 36
• Est. completion date: October 15, 2024
• Est. primary completion date: August 15, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years to 44 Years

Eligibility

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

Related Conditions & MeSH terms

• Epicondylitis of the Elbow
• Tennis Elbow

Intervention

Behavioral:
• mobilization
mobilization and exercise to be applied to patients with chronic lateral epicondylitis

Other:
• standard treatment
standard treatment
• deep friction
deep friction

Locations

Country	Name	City	State
Turkey	Yalova University	Yalova

Sponsors (1)

Lead Sponsor	Collaborator
Halic University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of Pain	In the assessment of pain, the "Visuel Analog Scale (VAS)" will be used and people will be asked to indicate the severity of their pain in the last 24 hours on a 10 cm chart. Before and after the session, VAS will be evaluated and recorded with the values measured with algometer. According to the pain scale in VAS application; "0" means no pain and "10" means the presence of unbearable pain, while patients will be asked to mark the pain they feel numerically between 0-10.	3 weeks
Primary	Quality of Life Short Form-36	The scale consists of 36 statements. The scale has 8 dimensions including physical functioning (FF), social functioning (SF), role limitations related to physical functioning (RRF), role limitations related to emotional problems (ERR), mental health (MS), vitality (C), bodily pain (BA) and general health perception (GS). Quality of life increases as the scores on the scale increase. Minimum score is 0 and maximum score is 100.	3 weeks
Primary	Assessment of Functionality	Duruöz Hand Index (DEI) specifically for rheumatoid arthritis patients. The index includes hand dexterity in the kitchen, during dressing, while maintaining personal hygiene, at work and other general movements. Participants rate 18 items from 0 (no difficulty) to 5 (impossible to do). The total score ranges from 0-90. A high score indicates impaired hand function.	3 weeks
Primary	Grip Strength	Grip strength will be evaluated with Jamar Hand Dynamometer. In the grip strength evaluations of the hand, measurements will be taken from both the patient and the healthy side. In the measurements made from the patient side, painless grip strength and maximum grip strength will be evaluated separately in the elbow flexion position and elbow extension position. On the healthy side, maximum grip strength will be evaluated in both positions. Patients will be positioned and evaluated according to the holding and gripping force of the dynamometer to be used. The patient will be asked to squeeze the dynamometer as strongly as possible for 5 seconds, first with the intact and then with the affected side, and 3 measurements will be made with one-minute breaks between the measurements and the averages will be recorded.	3 weeks