Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07382830

Effectiveness of a Visual Feedback Exercise Program Following Lumbar Surgery

Led by Suleyman Demirel University · Updated on 2026-02-03

42

Participants Needed

1

Research Sites

128 weeks

Total Duration

On this page

AI-Summary

What this Trial Is 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.

CONDITIONS

Official Title

Effectiveness of a Visual Feedback Exercise Program Following Lumbar Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 18 and 65 years old
  • Have undergone lumbar microdiscectomy surgery
  • Be able to read and write in Turkish
Not Eligible

You will not qualify if you...

  • Have had previous lumbar disc herniation surgery
  • Have had lumbar spine fusion surgery
  • Have a body mass index above 30
  • Have suspected or confirmed tumors in the lumbar spine or spinal canal
  • Have severe heart failure or cerebrovascular accident
  • Have cauda equina syndrome or other lumbar spine diseases
  • Have heart conditions, orthopedic contraindications, or systemic diseases preventing exercise participation
  • Refuse to participate in the study

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Antalya Provincal Health Directorate Antalya Training and Research Hospital

Antalya, Turkey (Türkiye)

Actively Recruiting

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Research Team

İ

İsmet Tümtürk, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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