Wearable Technological Device Applied to Patients with Chronic Pain
CompletedNot applicableNCT06345430
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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.
Study details
- Official title
- Clinical and Functional Effects of Wearable Technological Device Applied to Patients with Chronic Pain
- Interventions
- Device: Exopulse Molli-Suit (Wearable Technological Device)
- Sponsor
- Hacettepe University
- Start date
- 2023-12-18
- Primary completion
- 2024-04-15
- Sex
- All
- Age range
- from 20 Years to 65 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Being between the ages of 20-65 * Pain intensity should be at least 5 according to a numeric scale (low back pain and neck pain) * no pain for at least 6 months (healthy people) Exclusion Criteria: * Malignant condition, * People with systemic diseases such as neurological, psychological, cardiovascular, rheumatologic diseases and loss of function due to these diseases, * History of previous surgery on the spine and upper extremities, including the cervical and lumbar region, * Fractures in the spine and upper extremities, including the cervical and lumbar region, with a history of inflammation, * Acute infection, * Attending another rehabilitation program, * Refused to participate in the study and did not give written informed consent
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06345430