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Effectiveness of a Visual Feedback Exercise Program Following Lumbar Surgery

S

Suleyman Demirel University

Status

Enrolling

Conditions

Postoperative Rehabilitation
Randomized Controlled Trial
Lumbar Microdiscectomy

Treatments

Other: Control
Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT07382830
Laser Pointer Exercise

Details and patient eligibility

About

The aim of this study is to compare the effectiveness of stabilization exercises performed with visual feedback guided by a laser pointer after lumbar microdiscectomy surgery with that of standard stabilization exercises. The study, planned as a randomized controlled trial, will include 42 individuals aged 18-65 who have undergone lumbar microdiscectomy. Participants will be divided into two groups: a control group and a laser-guided exercise group. Both groups will undergo supervised stabilization exercises 3 days a week for 8 weeks, starting from the 6th postoperative week. The outcome measures were defined as pain, disability, back awareness, trunk muscle endurance, reaction time, balance, function, and lumbar proprioception. The findings are expected to demonstrate the effectiveness of visual feedback-assisted stabilization exercises in postoperative rehabilitation and contribute to clinical practice.

Full description

This study is a randomized controlled trial designed to compare the effects of stabilization exercises performed with laser-guided visual feedback and conventional stabilization exercises in individuals who have undergone lumbar microdiscectomy surgery. A total of 42 participants aged 18-65 years who have undergone lumbar microdiscectomy will be included in the study. Participants will be randomly assigned to either a control group or a laser-guided exercise group. Both groups will receive supervised stabilization exercise programs three times per week for eight weeks, starting from the sixth postoperative week. The exercise content will be similar in both groups, with the laser-guided group receiving additional visual feedback during exercises. Outcome measures will be assessed at baseline and after completion of the intervention. Assessments will include pain, disability, back awareness, trunk muscle endurance, reaction time, balance, functional performance, and lumbar proprioception. The results of this study are expected to contribute to evidence-based postoperative rehabilitation approaches following lumbar microdiscectomy.

Enrollment

42 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • To be between 18 and 65 years of age
  • Patients who underwent lumbar microdiscectomy surgery
  • Individuals who are literate in Turkish

Exclusion criteria

  • Patients who have previously undergone lumbar disc herniation surgery
  • The surgical procedure involving fusion has been performed.
  • Having a body mass index above 30
  • Suspected or confirmed tumors in the lumbar spine and spinal canal
  • Severe heart failure and cerebrovascular accident
  • The presence of cauda equina syndrome and concomitant diseases of the lumbar spine
  • The presence of heart conditions, orthopedic contraindications, or systemic diseases that could prevent participation in the exercise program
  • Refusing to participate in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

42 participants in 2 patient groups

Laser-Guided Exercise Group
Experimental group
Description:
Participants received a supervised stabilization exercise program guided by visual feedback using a laser pointer, in addition to standard postoperative care following lumbar microdiscectomy surgery.
Treatment:
Other: Exercise
Control Group
Active Comparator group
Description:
Participants received a supervised stabilization exercise program without standard postoperative care, back training, or visual feedback following lumbar microdiscectomy surgery.
Treatment:
Other: Control

Trial contacts and locations

1

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Central trial contact

İsmet Tümtürk, MSc

Data sourced from clinicaltrials.gov

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