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VR Training for Pilots With Neck Pain

Therapeutic Virtual Reality Training for Neck Pain in Israeli Air Force Pilots - A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02979041
Enrollment
47
Registered
2016-12-01
Start date
2016-09-01
Completion date
2017-12-30
Last updated
2018-05-24

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

Conditions

Cervical Pain, Neck Pain

Keywords

neck pain, Virtual reality, Range of motion, physiotherapy, Air force, kinematics

Brief summary

The aim of the proposed study is to investigate the effectiveness of an interactive, virtual reality (VR) training program for pilots compared with standard care. The study will be a randomized controlled trial (RCT) consisting of 60 pilots randomized into one of two groups: standard physiotherapy and medical care vs standard care and VR training. Outcome measures will include subjective scores of pain intensity and global perceived effect; objective measures of range of motion (ROM), neck motion velocity, and motion accuracy; and functional measure of days grounded due to neck pain. Data will be analyzed using ANOVA for within and between groups analyses.

Detailed description

The aim of the proposed study is to investigate the effectiveness of an interactive, virtual reality (VR) training program for pilots compared with standard care. The proposed intervention program includes training in neck range of motion, control, accuracy and coordination and is expected to reduce the prevalence and operational impact of neck pain in the intervention group more effectively than does standard care alone. The proposed study will be designed as a randomized, controlled trial (RCT). Sixty fighter and helicopter pilots will be randomized into two groups, to receive either standard physiotherapy and medical care or standard care with the addition of interactive, dynamic, controlled training (a self-exercise program) in VR to address the fast, accurate head control required in flying tasks. Subjective outcome measures will include pain intensity and global perceived effect. Objective measures will include range of motion, motion velocity and accuracy. The functional measure will include days grounded due to neck pain. Statistical analysis will use independent, repeated measures ANOVA on each parameter, within and between groups. Post hoc comparisons, including several preplanned contrasts, will be performed to assess differences before and after treatment, and the stability of changes over time, in each group. The relationship of risk factors to performance failures will be assessed using multivariate logistic regression analyses. This study is the first in the Israeli Air Force to evaluate this type of comprehensive, functional intervention program. Such research will dramatically advance the military's health care approach to neck pain, and may be further applied to other populations in and outside the Israeli Defence Force (IDF). This study may serve as a stepping stone to further research related to diagnosis, treatment, and prevention methods during a pilot's active service.

Interventions

BEHAVIORALInteractive virtual reality training

The proposed VR intervention program will provide active training to be performed individually 4 times a week for 20 minutes a session. The intervention program will be supervised by qualified, experienced physiotherapists, and will include individual training and two follow up meetings during the study period. The intervention program will include strengthening and endurance exercises for the cervical and shoulder girdle muscles. Training will include sensorimotor control and functional, quick, accurate, neck motion, using interactive VR training systems. This type of advanced training is very relevant to the pilots function in the cockpit as it includes interactive tasks aimed to increase range, speed, smoothness, accuracy, and control of cervical motion.

OTHERStandard Care

physiotherapy and medical care as provided currently

Sponsors

Medical Corps, Israel Defense Force
CollaboratorOTHER
University of Haifa
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* fighter and helicopter pilots from the Israeli Air Force * acute, sub-acute, and chronic neck pain, with or without referral to the upper limbs

Exclusion criteria

* neurological disorders (e.g. evidence for positive neurological signs), systemic disease, history of spinal surgery, or any disorders that may limit the ability to exercise

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity is measured using the Visual Analogue Scale (VAS, 0-100mm)change from baseline at 4 weeks, 3 and 6 months.Pain intensity was measured using the Visual Analogue Scale (VAS, 0-100mm)
Global perceived effect of the provided treatment is measured on a scale from -5 to +5.change from baseline at 4 weeks, 3 and 6 months.Global perceived effect of the provided treatment was measured on a scale from -5 to +5. Zero represented no change, +5 excellent improvement due to the treatment provided, and -5, vast worsening.
Functional outcome is measured by the number of grounding days from flying due to neck pain.change from baseline at 4 weeks, 3 and 6 months.The number of days the pilot was grounded due to neck pain.

Secondary

MeasureTime frameDescription
Cervical range of motion is measured using the neck VR system (ROM, degrees)change from baseline at 4 weeks, 3 and 6 months.Cervical range of motion (ROM, degrees) is measured using the neck VR system, into flexion, extension, right and left rotation.
Cervical motion velocity is measured using the neck VR system (degrees/second)change from baseline at 4 weeks, 3 and 6 months.Cervical motion velocity is measured using the neck VR system (degrees/second) into flexion, extension, right and left rotation.
Cervical muscles isometric strength is measures using a dynamometer (Newton)change from baseline at 4 weeks, 3 and 6 months.Cervical muscles isometric strength is measures using a dynamometer (Newton), in the directions of static flexion and extension.

Countries

Israel

Outcome results

None listed

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