Clinical Trials Logo

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


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
See also
  Status Clinical Trial Phase
Completed NCT01220505 - Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal System
Terminated NCT00974623 - Bone Graft Materials Observational Registry N/A
Withdrawn NCT02058238 - ADDRESS - Adult Deformity Robotic vs. Freehand Surgery to Correct Spinal Deformity
Recruiting NCT05323448 - Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion. N/A
Recruiting NCT05108948 - Research of Factors Determining the Improvement of Quality of Life at One Year of Adult Patients Treated for Spinal Deformity (COFTASD)
Completed NCT02950532 - Posterior Ligament Complex Assessment Without Magnetic Resonance Image in Thoracolumbar Fractures
Completed NCT01982045 - RCT of AttraX® Putty vs. Autograft in Instrumented Posterolateral Spinal Fusion N/A
Active, not recruiting NCT00738439 - Prospective, Multi-Center Adult Spinal Deformity Outcomes Database Registry
Completed NCT05579834 - Hemothorax Caused by Posterior Correction Surgery for Spinal Deformity
Completed NCT01608854 - Comparison of Antibiotic Protocols in Spine Patients With Postoperative Drains N/A
Active, not recruiting NCT04899297 - Quality of Life in Parents of Adolescents With Spinal Deformities: Development of a New Questionnaire.
Completed NCT05239962 - A Reliability And Validity Study Of The Urdu Version Of Spine Functional Index.
Active, not recruiting NCT05001893 - Clinical Safety and Efficacy of S53P4 Bioactive Glass Putty in Spinal Fusion Surgery
Completed NCT01601054 - Supplemental Anterior Lumbar Interbody Fusion (ALIF) in Spinal Deformity N/A
Active, not recruiting NCT04670536 - The Degen Study: Post-market Clinical Follow-up on the PASS LP, PASS Degen and PASS Tulip Systems (PASS DEGEN)
Completed NCT03880292 - Spinal Deformity Intraoperative Monitoring. N/A
Recruiting NCT05856370 - The Ailliance Post-Market Clinical Study N/A
Recruiting NCT05146193 - AI-Powered Scoliosis Auto-Analysis System Multicenter Development and Validations
Active, not recruiting NCT04642456 - Balance Assessment Scale and Strength Measurement Protocol to Measure Functionality in Adults With Spinal Deformity N/A
Recruiting NCT04071665 - A Modified Lateral Lumbar Interbody Fusion VS. Transforaminal Lumbar Interbody Fusion for Adult Degenerative Scoliosis N/A