Virtual Reality and Cervical Mobilization

Neck Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05829564
• Other study ID #: VRMOB
• Status: Completed
• Phase: N/A
• Start date: May 10, 2023
• Est. completion date: September 15, 2023

Study information

• Verified date: March 2024
• Source: Hacettepe University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: September 15, 2023
• Est. primary completion date: June 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Neck Pain
• Virtual Reality

Intervention

Other:
• virtual reality
The individuals participating in the study will experience virtual reality.
• cervical mobilization
The individuals participating in the study will be applied cervical mobilization techniques.
• exercise
The individuals participating in the study will performed neck-specific exercises.

Locations

Country	Name	City	State
Turkey	Hacettepe University	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Joint position sense error	Proprioception in all cervical directions will assessed by Cervical Range of Motion device.	Change from Baseline balance after 4 weeks/10 sessions.
Primary	Baropodometer assessments-Pressure distribution	Pressure distribution will assess with FreeMed baropodometric platform and will record as percentage.	Change from Baseline proprioception after 4 weeks/10 sessions.
Primary	Baropodometer assessments- Center of gravity	Center of gravity will assess with FreeMed baropodometric platform and will record as mm.	Change from Baseline proprioception after 4 weeks/10 sessions.
Primary	Baropodometer assessments- Oscillations	Oscillations will assess with FreeMed baropodometric platform.	Change from Baseline proprioception after 4 weeks/10 sessions.
Primary	Baropodometer assessments- Sway velocity	Sway velocity will assess with FreeMed baropodometric platform and will record as degrees.	Change from Baseline proprioception after 4 weeks/10 sessions.
Primary	Functional Balance	10 meter walking speed and four square step-test will be combined to report dynamic balance.	Change from Baseline proprioception after 4 weeks/10 sessions.
Secondary	Cervical Pain	Visual Analog Scale will be used to assess this outcome measure.	Change from Baseline cervical pain after 4 weeks/ 10 sessions.
Secondary	Functional disability	Neck Disability Index will be used to assess this outcome measure.	Change from Baseline functional disability after 4 weeks/ 10 sessions.
Secondary	quality of life about cervical pain	SF-36 will be used to assess this outcome measure.	Change from Baseline quality of life about cervical pain after 4 weeks/ 10 sessions.
Secondary	Global perceived effect	Global perceived effect scale will be used to assess this outcome measure/ 10 sessions.	Change from Baseline Global perceived effect after 4 weeks/ 10 sessions.