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NCT06190873 Clinical Trial

The Effect of Telephone Education on Fear of Movement and Quality of Life in Patients With Lumbar Disc Herniation Surgery.

Spinal Deformity Clinical Trial

Official title:
Effect of Telephone Training on Fear of Movement and Quality of Life in Patients With Lumbar Disc Herniation Surgery: Randomized Controlled Study.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06190873
Other study ID # COMÜ- SBF-NT-01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2023
Est. completion date January 1, 2025

Study information
Verified date December 2023
Source Çanakkale Onsekiz Mart University
Contact Nilgun Temel
Phone 05466520892
Email nilgun.yavas91@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim is to quantify the fear of movement and quality of life of telephone education on lumbar disc herniation surgery.

Description:

In the randomized controlled study, patients will be randomized into two categories: experimental and control groups. The experimental group will receive intervention via online information for 6 weeks after discharge. The control group will not be given online training other than standard nursing care. At the end of 6 weeks, the difference between fear of movement and quality of life between the two groups will be examined.

Recruitment information / eligibility
Status Recruiting
Enrollment 80
Est. completion date January 1, 2025
Est. primary completion date January 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - being over 18 years old - knowing how to read and write Turkish - No hearing or speech impairment - Having lumbar disc herniation surgery for the first time - having a personal cell phone - being discharged 5 days after surgery Exclusion Criteria: - being under 18 years old - being illiterate - having a hearing and speech disability - not having a personal cell phone - staying in the hospital for more than 5 days after surgery

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• post-discharge rehabilitation training
Telephone training will be provided for post-discharge rehabilitation

Locations
Country Name City State
Turkey Çanakkale Mehmet Akif Ersoy Devlet Hastenesi Çanakkale

Sponsors (1)
Lead Sponsor Collaborator
Çanakkale Onsekiz Mart University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary movement fear scale In the measurement to be made with a four-point Likert type scale, 17 is the lowest score and 68 is the highest score. The higher the score the patient receives, the greater the fear of movement. six week
Secondary quality of life scale The score obtained from the scale varies between 0 and 100. As the score obtained from the scale increases, the patient's quality of life increases. six week
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