CI

At a glance

ClinicalIndex Comparison Record
N/ARecruiting· 93 target
Drug / intervention
Virtual Reality +2 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06397157
NCT06397157N/ARecruitingUpdate OverdueUpdated 24mo ago · Completion was 24mo ago
Enrollment Stalled
Update Overdue

Combined Effects of Virtual Reality and Motor Imagery With Routine Physical Therapy in Patients With Non-specific Neck Pain

Riphah International University·interventional·Posted May 2, 2024·Updated Jun 13, 2024

In Brief

A clinical study evaluating Virtual Reality, Motor Imagery, and 1 other intervention for Cervical Pain and 2 related conditions. Currently recruiting, targeting 93 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

Non-specific neck pain is the most common musculoskeletal symptom which can cause limited cervical mobility, impaired functional status and stress at work. Virtual reality and motor imagery are unique technologies which have beneficial effects on the treatment of non-specific neck pain. Virtual reality is a simulated 3D environment that enables users to explore and interact with a virtual surrounding while motor imagery (MI) is a dynamic mental process of an action, without its actual motor execution. This study aims to investigate the combined effects of Virtual Reality (VR) and Motor Imagery Techniques (MI) with Routine Physical Therapy (RPT) in patients with Non-specific neck pain. This randomized clinical trial will be carried at Railway General Hospital, Rawalpindi on 93 participants meeting the inclusion criteria included in the study through probability convenience sampling technique. 3 groups of participants assigned ramdomly will receive interventions for three days a week for 6 weeks. Group A will receive virtual reality (VR) and motor imagery (MI) along with routine physical therapy for . Group B participants will receive VR along with routine physical therapy while Group C will receive MI along with routine physical therapy. Total treatment time will be 40 minutes. Outcome measure tools will be Numeric pain rating scale to measure pain, the Tampa scale of Kinesiophobia (TSK) for the measurement of kinesiophobia and Neck disability index for disability and functional status.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPakistan
Collaborators--

Timeline

N/ARecruitingOverdue
202420252026
First PostedMay 2, 2024
Enrollment StartDec 10, 2023
Primary CompletionJun 10, 2024
Study CompletionJul 10, 2024
TodayJul 1, 2026
Enrollment to primary: 6 monthsPosted 2.2 years ago

Interventions

Virtual Realityother

Participants will recieve treatment(Virtual reality) for every alternate day (3 days per week) for 6 weeks. Total number of sessions will be 18.

Motor Imageryother

Participants will recieve treatment(Motor Imagery) for every alternate day (3 days per week) for 6 weeks. Total number of sessions will be 18.

Routine Physical therapyother

Participants will recieve treatment(Routine physical therapy) for every alternate day (3 days per week) for 6 weeks. Total number of sessions will be 18.