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The project will evaluate thermoregulatory processes among individuals with and without first-episode psychosis.
Full description
The project will evaluate thermoregulatory processes among individuals with and without first-episode psychosis.
Aim 1: Assess whether individuals with first-episode psychosis have differences in mean temperature and diurnal temperature variation as compared to individuals without psychosis.
Aim 2: Examine whether mean temperature and temperature variation during periods of rest and activity are different between individuals with first-episode psychosis versus people without psychosis.
Aim 3: Explore the association between current core body temperature and current ratings of psychotic symptomatology among individuals with first-episode psychosis.
Study participants will complete baseline assessments (e.g., symptoms, functioning, and sleep) and then complete a 24-36 hour ambulatory assessment period in which core temperature, activity, sleep, and heart rate variability will be tracked continuously and symptom severity will be assessed sporadically using a symptom rating app on their smart phone. .Then they will complete a second study visit to repeat baseline assessments.
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Volunteers
Inclusion and exclusion criteria
Eligibility for Individuals with First-Episode Psychosis:
Eligibility for Individuals without First-Episode Psychosis:
Eligibility for Individuals with and without First-Episode Psychosis:
Ages 18 - 35
No evidence of swallowing difficulties as assessed using the Swallowing Disturbance Questionnaire [SDQ]. defined as (i) a score <5 on the SDQ oral phase questions, (ii) a score <11.5 on the laryngopharygeal phase SDQ questions, and a total SDQ score < 12.5.
Not meeting diagnostic criteria for a substance use disorder over the past month as determined using the Structured Clinical Interview for the DSM-5 .
No current or past diagnosis of a medical condition known to affect thermoregulatory Functioning as assessed using the Health Conditions that Affect Thermoregulation questionnaire
Per recommendations from the manufacturer of the CorTemp continuous temperature sensor, we will not enroll:
0 participants in 2 patient groups
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Central trial contact
Nicholas Breitborde, PhD
Data sourced from clinicaltrials.gov
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