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RecruitingNCT06190873Updated Jan 5, 2024

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

An interventional study of post-discharge rehabilitation training in Spine Disease and Spinal Deformity, sponsored by Çanakkale Onsekiz Mart University. Recruiting at 1 site in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-01-05.

Sponsored by Çanakkale Onsekiz Mart University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the detailed 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.

02

Conditions studied

  • Spine Disease
  • Spinal Deformity

Keywords

  • life quality
  • telehealty
  • tele nursing
  • kinezyofobi
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
04

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    group to be trained over the phone

    This group will be trained by phone for 6 weeks after discharge.

    Behavioral: post-discharge rehabilitation training

  • No intervention
    Group without telephone training

    This group will be given training during their stay in the hospital. There will be no training over the phone after discharge.

Interventions

  • Behavioralpost-discharge rehabilitation training

    Telephone training will be provided for post-discharge rehabilitation

    Also known as: nursingcare, nursing education

05

What researchers measure

Primary outcomes

  1. 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.

    Time frame: six week

Secondary outcomes

  1. 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.

    Time frame: six week

06

Study locations

1 of 1 sites recruiting
  • Çanakkale Mehmet Akif Ersoy Devlet Hastenesi
    Çanakkale, 17100, Turkey
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06190873
Lead sponsor
Çanakkale Onsekiz Mart University
Responsible party
Nilgün Temel (graduate student, Çanakkale Onsekiz Mart University) — Principal investigator
First posted
Jan 5, 2024
Start date
Dec 1, 2023
Primary completion
Jan 1, 2025 (estimated)
Completion
Jan 1, 2025 (estimated)
Last update
Jan 5, 2024

Study contacts

Nilgun Temel
Contact
nilgun.yavas91@gmail.com
05466520892

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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