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Results of Cervical Segmental Mobilization in Patients With Chronic Lateral Epicondylitis

Investigation of the Effect of Cervical Segmental Mobilization on Pain, Functionality, Grip Strength and Quality of Life in Patients With Chronic Lateral Epicondylitis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06440928
Enrollment
36
Registered
2024-06-04
Start date
2024-05-15
Completion date
2024-10-15
Last updated
2024-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epicondylitis of the Elbow, Servical Segmental Mobilization

Keywords

Lateral epicondylitis, Servical segmental mobilization, Pain, Quality of life, Grip strenght, Functionality

Brief 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.

Interventions

BEHAVIORALmobilization

mobilization and exercise to be applied to patients with chronic lateral epicondylitis

OTHERstandard treatment

standard treatment

OTHERdeep friction

deep friction

Sponsors

Halic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

randomised controlled and experimental study

Eligibility

Sex/Gender
ALL
Age
25 Years to 44 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Pain3 weeksIn 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.
Quality of Life Short Form-363 weeksThe 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.
Assessment of Functionality3 weeksDuruöz 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.
Grip Strength3 weeksGrip 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.

Countries

Turkey (Türkiye)

Contacts

Primary Contactmustafa yığılıtaş, doctorate
fztmy77@hotmail.com05309782720
Backup Contactseda saka, asst.prof
seda.saka@halic.edu.tr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026