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About
The objective of this study is to evaluate the cortisol awakening response with persons with Parkinsons Disease (PD), Huntingtons Disease (HD), and controls. These data are desired so experience can be gained with measuring stress levels subjectively and objectively in persons with PD, HD, and controls.
Full description
Telephone consent will be obtained.
Participants will collect saliva at twelve time points - four times a day for three days.
Visits will be conducted virtually (over the internet).
The virtual visit is to assess Parkinson's or Huntington's disease status, stress, mood, and quality of life.
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Group (3) Inclusion:
Group (5) Inclusion:
Group (6) Inclusion:
Group (7) Inclusion:
Exclusion criteria
131 participants in 7 patient groups
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Central trial contact
Susan M O'Connor, RN; Brenna M Lobb, MS, MPH
Data sourced from clinicaltrials.gov
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