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Clinical Trials/NCT05829564
NCT05829564CompletedNot Applicable

Comparison of the Effects of Virtual Reality and Cervical Mobilization in Individuals With Chronic Neck Pain

Hacettepe University2 sites in 2 countries52 target enrollmentStarted: May 10, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
2
Primary Endpoint
Joint position sense error

Study Overview

Brief Summary

The aim of this study is to compare the effects of virtual reality and cervical mobilization on proprioception, balance parameters, pain, disability level, quality of life and overall felt effect in individuals with chronic neck pain. In addition, it is aimed to qualitatively evaluate the virtual reality perspectives of individuals with chronic neck pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Neck pain persisting for at least 3 months
  • Being between the ages of 18-65,
  • Being sedentary (not included in any physical therapy program in the last 6 months), ->10 points from the Neck Disability Index

Exclusion Criteria

  • History of previous spinal surgery
  • Neurological, cardiopulmonary, musculoskeletal disease affecting physical performance
  • Any pathology in the shoulder joint
  • Spinal trauma history
  • Pregnancy

Outcomes

Primary Outcomes

Joint position sense error

Time Frame: Change from Baseline balance after 4 weeks/10 sessions.

Proprioception in all cervical directions will assessed by Cervical Range of Motion device.

Baropodometer assessments-Pressure distribution

Time Frame: Change from Baseline proprioception after 4 weeks/10 sessions.

Pressure distribution will assess with FreeMed baropodometric platform and will record as percentage.

Baropodometer assessments- Sway velocity

Time Frame: Change from Baseline proprioception after 4 weeks/10 sessions.

Sway velocity will assess with FreeMed baropodometric platform and will record as degrees.

Baropodometer assessments- Center of gravity

Time Frame: Change from Baseline proprioception after 4 weeks/10 sessions.

Center of gravity will assess with FreeMed baropodometric platform and will record as mm.

Baropodometer assessments- Oscillations

Time Frame: Change from Baseline proprioception after 4 weeks/10 sessions.

Oscillations will assess with FreeMed baropodometric platform.

Functional Balance

Time Frame: Change from Baseline proprioception after 4 weeks/10 sessions.

10 meter walking speed and four square step-test will be combined to report dynamic balance.

Secondary Outcomes

  • quality of life about cervical pain(Change from Baseline quality of life about cervical pain after 4 weeks/ 10 sessions.)
  • Global perceived effect(Change from Baseline Global perceived effect after 4 weeks/ 10 sessions.)
  • Cervical Pain(Change from Baseline cervical pain after 4 weeks/ 10 sessions.)
  • Functional disability(Change from Baseline functional disability after 4 weeks/ 10 sessions.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

HATİCE ÇETİN

Assist, Prof

Hacettepe University

Study Sites (2)

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