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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.