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

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

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06190873

Enrollment

Registered

2024-01-05

Start date

2023-12-01

Completion date

2025-01-01

Last updated

2024-01-05

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

Conditions

Spinal Deformity, Spine Disease

Keywords

life quality, telehealty, tele nursing, kinezyofobi

Brief summary

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

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.

Interventions

BEHAVIORALpost-discharge rehabilitation training

Telephone training will be provided for post-discharge rehabilitation

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

DOUBLE (Subject, Outcomes Assessor)

Masking description

Participants will not know which group they belong to.

Intervention model description

There will be two groups, one is the control group and the other is the intervention group.

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

* 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

Design outcomes

Primary

Measure	Time frame	Description
movement fear scale	six week	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.

Secondary

Measure	Time frame	Description
quality of life scale	six week	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.

Countries

Turkey (Türkiye)

Contacts

Primary ContactNilgun Temel

nilgun.yavas91@gmail.com05466520892

Outcome results

None listed

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