Using virtual reality to improve shoulder function after neck surgery
Virtual Reality For Shoulder Dysfunction Post Neck Dissection Surgeries
This study is testing if virtual reality therapy can help people recover better and feel less pain in their shoulders after neck surgery compared to regular physical therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 68 (estimated) |
| Ages | 40 Years to 60 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza, Dokki) |
| Trial ID | NCT06257238 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of virtual reality in alleviating pain and improving shoulder function in patients who have undergone neck dissection surgeries. A total of 68 participants, aged 40-60, will be randomly assigned to either a study group receiving virtual reality therapy or a control group receiving traditional physical therapy. Both groups will undergo treatment twice a week for two months, with assessments conducted before and after the intervention to measure pain levels and range of motion. The study utilizes immersive technology to potentially enhance rehabilitation outcomes for shoulder dysfunction.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 40-60 who have experienced shoulder dysfunction after neck dissection surgery.
Not a fit: Patients outside the age range of 40-60, those with hearing or visual impairments, or individuals with acute viral diseases or mental disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and functional recovery for patients with shoulder dysfunction following neck dissection surgeries.
How similar studies have performed: While the use of virtual reality in rehabilitation is gaining traction, this specific application for shoulder dysfunction post-neck dissection is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age range between 40-60 years * Both genders will participate in the study * All patients have undergone neck dissection surgery * All patients enrolled to the study will have their informed consent Exclusion Criteria: * Age more than 60 years or less than 40 years * Subjects who have hearing problems * Subjects who have visual problems * Patients have acute viral diseases, acute tuberculosis, mental disorders or those with pace makers
Where this trial is running
Giza, Dokki
- Faculty of Physical Therapy — Giza, Dokki, Egypt (Recruiting)
Study contacts
- Study coordinator: H K Aly, Master
- Email: drhayaakhaled@gmail.com
- Phone: 01094012699
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.