VisszavonvaFázis nélkül
Measurement of Osteoarthritic Patient Pain Through Electrodermal Activity Signals
A legfontosabb adatok
- Ki végzi
- Dartmouth-Hitchcock Medical Center
- Hol
- Lebanon (Egyesült Államok)A helyszín megnézése
- Azonosító
- Állapot
- Visszavonva
- Kezdés
- 2026. aug.
- Befejezés
- 2026. okt.
- A vizsgálat típusa
- Beavatkozással járó
- A vizsgált kezelések
- Electrodermal Activity signal
- A regiszteradat frissítve
- 2026. november 13.
- Miért állt le
- The study was not pursued
Ki vehet részt
- Életkor
- 50 év – 80 év
- Nem
- Nők és férfiak
- Egészséges önkéntesek
- Részt vehetnek
A regiszter feltételei, szó szerint
Mind a 13 feltétel megnézéseKevesebb
Ki vehet részt
- Kellgren-Lawrence Grade >= 3
Ki nem vehet részt
- Prior history of knee surgery, knee injections, or injury to knee joints (e.g., meniscus tears, ligamentous injuries), BMI >=35; Both groups, exclusion:
- Subjects with chronic heart problems, including, but not limited to, chronic hypertension, heart palpitations, a weak or irregular heartbeat, or a previous heart attack,
- Subjects taking the following drugs within 12 hours of the experiment or during the experiment: caffeine, alcohol, psychoactive drugs, nicotine or marijuana, other recreational drugs, and medicine of any kind that is not normally taken daily. Such medications include; NSAIDs; Acetaminophen; Steroidal anti-inflammatory agents; Bronchodilators; Appetite suppressants; Lipase inhibitors
- Subjects with Raynaud's syndrome
- Subjects with any of the following conditions: active skin lesions where EDA sensors are, vertigo or dizziness, and anyone with postural orthostatic tachycardia syndrome (POTS), peripheral neuropathy, seizure disorders, methicillin-resistant staphylococcus aureus (MRSA), impaired circulation, medical implants, open skin lesions, chronic eczema on hands where EDA and electrical stimulator's electrodes are attached, diabetes, and epilepsy
- Participants who cannot feel physical pain or have a history of self-harm
- Inflammatory arthropathy (e.g., rheumatoid arthritis), BMI >=35; Control subjects:
- Complaints of lower extremity joint pain
- Known diagnosis of knee osteoarthpathy
- Women who are currently pregnant
- Participants who have a skin sensitivity to metals, have a pacemaker or defibrillator, or have recent head trauma within the past two weeks (even without loss of consciousness)
Egyéb feltételek
- Study subjects
Helyszínek itt: Egyesült Államok
- Dartmouth Hitchcock Medical CenterLebanon, Egyesült ÁllamokNo longer taking part
A vizsgálatról
Mit akar kideríteni a vizsgálat
This pilot study aims to investigate the viability of using a smartwatch-based electrodermal activity (EDA) sensor to capture enough EDA signal to quantitatively assess pain in osteoarthritis subjects and test the feasibility of its methods and procedures for later use in subsequent larger-scale studies.
A vizsgálat csoportja
- Electrodermal Activity Measurement SubjectsA vizsgált kezelés
Participants will have their baseline electrodermal activity (EDA) response to pain measured as well as their EDA response measured while participating in a set of standardized functional tests.
Kezelés: Electrodermal Activity signal
Adatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- A regiszteradat frissítve
- 2026. november 13.