Effectiveness of Home Programs After Lumbar Spinal Decompression Surgery

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-14

Study Completion Date

2024-04-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The study will be conducted with volunteer patients who are followed up by Bursa Çekirge State Hospital Cekirge State Hospital Neurosurgery outpatient clinic and who have undergone lumbar decompression surgery and who meet the study criteria. The cases will be divided into 2 groups by randomization software. The control group will receive post-operative exercise training and will be encouraged to move. The study group will receive a core stabilization program in addition to education via telerehabilitation. The first evaluation will be performed 2 months post-operatively and the second evaluation will be performed 2 months after treatment.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Efficacy of Motor Control Exercise Program After Lumbar Spinal Decompression Surgery

NCT06014632

Lumbar Spine Disease

COMPLETED NA

Exercise After Lumbar Disc Herniation Surgery

NCT06046781

Disc Herniation Surgery

COMPLETED NA

Investigation of the Effectiveness of Dynamic Neuromuscular Stabilization Exercises After Lumbar Disc Herniation Surgery

NCT06005948

Low Back Pain Kinesiophobia

COMPLETED NA

Development of a Fascial Training Based Mobile Application and Investigation of Its Effectiveness in Patients With Disc Herniation

NCT07060235

Lumbar Disc Disease Lumbal Disc Herniation

ENROLLING_BY_INVITATION NA

The Effect of Preoperative Turning in Bed and Mobilization Training on the Postoperative First Mobility

NCT04674215

Postoperative Mobility

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Lumbar Spine Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention Group

This program will include reeducation isometric contraction exercises for transversus obdominus, oblique abdominals, multifidus lumborum muscles and strengthening stretching exercises for other extremities. These interventions will be sent to the patients via telerehabitation method and the patients will always have access to the programs and training.

Group Type EXPERIMENTAL

Rehabilitation

Intervention Type OTHER

The study group will be given a core stabilization program in addition to education.

Control Group

The control group will receive post-operative exercise training and will be encouraged to move as described by Moseley et al., 2004.

Group Type ACTIVE_COMPARATOR

Control

Intervention Type OTHER

The control group will receive post-operative cognitive training and will be encouraged to move.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Rehabilitation

The study group will be given a core stabilization program in addition to education.

Intervention Type OTHER

Control

The control group will receive post-operative cognitive training and will be encouraged to move.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Having undergone lumbar decompression surgery without fusion and 2 months of history
* Participate in all necessary follow-up assessments
* Being between 18-65 years old
* Understand simple commands
* Signing the consent form

Exclusion Criteria

* Presence of a previous spinal fusion surgery
* Presence of malignancy
* Having undergone spine surgery before
* Have any other orthopedic or neurological problem that may affect treatment and assessments
* Situations that prevent communication
* Lack of cooperation during the study

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No