Skip to content

Virtual Reality and Cervical Mobilization

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05829564
Enrollment
52
Registered
2023-04-25
Start date
2023-05-10
Completion date
2023-09-15
Last updated
2024-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain, Virtual Reality

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.

Interventions

OTHERvirtual reality

The individuals participating in the study will experience virtual reality.

The individuals participating in the study will be applied cervical mobilization techniques.

OTHERexercise

The individuals participating in the study will performed neck-specific exercises.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Functional BalanceChange from Baseline proprioception after 4 weeks/10 sessions.10 meter walking speed and four square step-test will be combined to report dynamic balance.
Baropodometer assessments-Pressure distributionChange from Baseline proprioception after 4 weeks/10 sessions.Pressure distribution will assess with FreeMed baropodometric platform and will record as percentage.
Baropodometer assessments- Center of gravityChange from Baseline proprioception after 4 weeks/10 sessions.Center of gravity will assess with FreeMed baropodometric platform and will record as mm.
Baropodometer assessments- OscillationsChange from Baseline proprioception after 4 weeks/10 sessions.Oscillations will assess with FreeMed baropodometric platform.
Baropodometer assessments- Sway velocityChange from Baseline proprioception after 4 weeks/10 sessions.Sway velocity will assess with FreeMed baropodometric platform and will record as degrees.
Joint position sense errorChange from Baseline balance after 4 weeks/10 sessions.Proprioception in all cervical directions will assessed by Cervical Range of Motion device.

Secondary

MeasureTime frameDescription
Functional disabilityChange from Baseline functional disability after 4 weeks/ 10 sessions.Neck Disability Index will be used to assess this outcome measure.
quality of life about cervical painChange from Baseline quality of life about cervical pain after 4 weeks/ 10 sessions.SF-36 will be used to assess this outcome measure.
Global perceived effectChange from Baseline Global perceived effect after 4 weeks/ 10 sessions.Global perceived effect scale will be used to assess this outcome measure/ 10 sessions.
Cervical PainChange from Baseline cervical pain after 4 weeks/ 10 sessions.Visual Analog Scale will be used to assess this outcome measure.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026