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Investigating the Augmented Effects of Virtual Reality Training in Patients Who Have Undergone Lumbar Spine Discectomy Surgery

Investigating the additional effects of virtual reality exercises on pain, fear of movement, disability and physical performance in patients who have undergone lumbar spine discectomy surgery: A randomized controlled clinical trial study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241208063981N1
Enrollment
48
Registered
2024-12-15
Start date
2025-01-11
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

People who have undergone lumbar discectomy surgery to relieve pressure on the nerve roots..

Interventions

Intervention 1: Intervention group: Virtual reality therapy exercise with lumbar spine stability exercises. The virtual reality equipment used as an intervention in this study includes a Meta Quest VR

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: Age between 20 and 55 years Have undergone their first lumbar disc herniation surgery Have sufficient language abilities and appropriate mental functions to understand and respond to the therapist Patients who have had lumbar spine surgery for four weeks Having at least a junior high school diploma Having a minimum pain of 3 and a maximum pain of 7 on the VAS scale

Exclusion criteria

Exclusion criteria: Having previous spine and lower limb surgery Pregnancy epilepsy Neurological problems and other problems that have prevented the person from being able to walk and perform functional tests and have been confirmed by a doctor (Parkinson's, wheelchair-bound people, severe cognitive diseases, severe cardiovascular diseases, stroke) Inability to fill out the questionnaire Lack of understanding of Persian language Visible scoliosis Problems with the vestibular system and postural vertigo (balance control) Spinal instability such as spondylolisthesis Problems such as infection, tumor, inflammatory disease, cardiovascular, pulmonary, or metabolic disorders, and diabetes Body mass index greater than 30

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: Visual Analog Scale Questionnaire.;Disability. Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: Oswestry Disability Index Questionnaire.;Fear of movement (Kinesiophobia). Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: Tampa Scale of Kinesiophobia.;Physical performance. Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: time up and go test.

Secondary

MeasureTime frame
Balance. Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: Modified STAR Excursion Balance Test.;Quality of life. Timepoint: Immediately before treatment, after treatment and 4 weeks after treatment. Method of measurement: 12-Item Short Form Survey.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Mollaei Barejahri

Shiraz University of Medical Sciences

ptalireza1@gmail.com+98 76 3222 0265

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026