ClinicalTrials.Veeva

Menu

Effectiveness of Home Programs After Lumbar Spinal Decompression Surgery

M

Muğla Sıtkı Koçman University

Status

Completed

Conditions

Lumbar Spine Disease

Treatments

Other: Rehabilitation
Other: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT06014645
Bursa NRŞ RKÇ

Details and patient eligibility

About

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.

Enrollment

22 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

22 participants in 2 patient groups

Intervention Group
Experimental group
Description:
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.
Treatment:
Other: Rehabilitation
Control Group
Active Comparator group
Description:
The control group will receive post-operative exercise training and will be encouraged to move as described by Moseley et al., 2004.
Treatment:
Other: Control

Trial contacts and locations

1

Loading...

Central trial contact

Fatih Özden, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems