Actively Recruiting
Regulation of Affect and Physiology in Depression
Led by University of Southern California · Updated on 2026-05-04
252
Participants Needed
1
Research Sites
218 weeks
Total Duration
On this page
Sponsors
U
University of Southern California
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Although treatments for depression are effective for many people, not everyone responds to treatment. This lack of treatment response could be due, in part, to the presence of multiple underlying causes of people's depression. This study aims to identify subtypes of depression, based on two factors: how successful people perceive themselves to be at regulating their affect in everyday life; and how much activity in the parasympathetic nervous system increases during moments when people try to regulate. The study involves ambulatory assessment of affect, regulation strategies, and physiological activity in everyday life, in a sample of young adults with remitted major depressive disorder and healthy volunteers. We will study regulation responses in the lab to further determine how subtypes differ in neural, physiological, and behavioral responses. Finally, participants will be randomly assigned to a remote, self-administered biofeedback intervention (vs. control intervention) designed to increase parasympathetic activity and physiological regulation success. While engaging in biofeedback at home for 10 days, participants will simultaneously repeat the ambulatory assessments. This design will allow us to determine the proximal impact of biofeedback on indices of regulation success in everyday life, and whether biofeedback has differential impact on regulation success for different subtypes.
CONDITIONS
Official Title
Regulation of Affect and Physiology in Depression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 27 years
- For participants with remitted depression: lifetime diagnosis of major depressive disorder
- Currently in full remission with no significant symptoms for at least eight weeks and a Hamilton Depression Rating Scale score of 7 or less
- For healthy volunteers: no lifetime history of psychiatric disorders
- For healthy volunteers: no first-degree relatives with mood disorders
You will not qualify if you...
- Change in psychotropic medication within the last 30 days
- Diagnosis of autism spectrum disorder
- Current eating disorder
- Intellectual disability
- Substance use disorder within the past 6 months
- Contraindications for MRI or ECG assessments such as metal in the body, claustrophobia, cardiac device, or pregnancy
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Southern California
Los Angeles, California, United States, 90089
Actively Recruiting
Research Team
U
Umiemah Farrukh
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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