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Investigation of the Efficacy of Treatments With Backup Device in Spine Pathologies

U

Uskudar University

Status

Completed

Conditions

Back Pain
Disc Herniation
Spine Disease
Neck Pain

Treatments

Other: conventional physiotherapy
Other: Backup therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06006377
Uskudar56

Details and patient eligibility

About

Our aim in this study is to examine the effectiveness of the Backup spine health device in spinal problems and compare it with traditional physical therapy methods.

Full description

The investigators study was planned as a randomized controlled study. Participants will be divided into 2 groups as conventional physiotherapy and Backup group by simple randomized method. Participants will be taken to a treatment program for 10 weeks, 3 days a week. Parameters such as pain, posture, sleep quality, quality of life, muscle shortening at the beginning and end of the study. The results will be analyzed statistically.

Enrollment

30 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being between the ages of 20-60
  • sick individuals with spinal problems
  • Persons who have filled out the consent form

Exclusion criteria

  • People with spinal pathology for whom physiotherapy is contraindicated
  • Having a neurological problem

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

conventional
Active Comparator group
Description:
conventional physiotherapy methods
Treatment:
Other: conventional physiotherapy
backup
Experimental group
Description:
Physiotherapy applied with backup device
Treatment:
Other: conventional physiotherapy
Other: Backup therapy

Trial contacts and locations

1

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Central trial contact

ömer şevgin

Data sourced from clinicaltrials.gov

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