NCT06345430

Wearable Technological Device Applied to Patients with Chronic Pain

Clinical and Functional Effects of Wearable Technological Device Applied to Patients with Chronic Pain

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Hacettepe University · Academic / Other
• Sex: All
• Age: 20 Years – 65 Years
• Healthy volunteers: Accepted

Summary

Within the scope of this research, a single session of Wearable Technological Device (Exopulse Molli-Suit) will be applied to patients with chronic back and neck pain. The results will be evaluated acutely, after 24 hours, after 1 week and after 1 month.

Detailed description

After initial evaluations, patients received a single session for 1 hour. Exopulse Mollii Suit will be applied. The stimulation level of the electrodes will be determined by the automatically by the system in accordance with the level of pain they indicate for their parts, individually tailored to the person. will be created. Patients will wear the Exopulse Mollii Suit, which is suitable for their body size, Hacettepe University Physics They will dress in the room allocated for them at the Faculty of Treatment and Rehabilitation. After each use The hygiene of Exopulse Mollii Suits has been evaluated at Hacettepe University Faculty of Physical Therapy and Rehabilitation in this will be provided with the help of a special device included in the scope. Initial assessments will be made immediately will be repeated three more times: after the intervention, 24 hours after the intervention and 4 weeks after the intervention. All data will be collected face-to-face from patients using the instruments mentioned above.

Conditions

• Neck Pain
• Low Back Pain
• Chronic Pain
• Musculoskeletal Pain

Interventions

Type	Name	Description
DEVICE	Exopulse Molli-Suit (Wearable Technological Device)	After initial evaluations, patients will receive Exopulse Mollii Suit in a single session for 1 hour. The stimulation level of the electrodes will be automatically generated by the system in accordance with the pain level specified by the patients for their body parts before the application.

Timeline

• Start date: 2023-12-18
• Primary completion: 2024-04-15
• Completion: 2024-06-30
• First posted: 2024-04-03
• Last updated: 2025-01-20

Locations

1 site across 1 country: Turkey (Türkiye)