PERsonalized Mood Augmentation Trial for Depressed Mood
NCT ID: NCT05662254
Last Updated: 2025-03-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2022-06-01
2024-10-11
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Audio-based Mental Health Intervention Study
NCT05555745
Mood Management Effects of Brief Unsupported Internet Interventions II
NCT02789280
Meditative Neurofeedback for Depression
NCT06675240
Assessing Improvements in Mood and Sleep Trial
NCT06639477
Psychopharmacotherapy for Depressive Patients
NCT06054321
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Personalized Behavioral Intervention
Behavioral lifestyle intervention assigned according to each participant's mood and lifestyle data patterns.
Personalized Behavioral Intervention
Behavioral lifestyle intervention assigned according to each participant's mood and lifestyle data patterns.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Personalized Behavioral Intervention
Behavioral lifestyle intervention assigned according to each participant's mood and lifestyle data patterns.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* psychotic disorders
* bipolar disorder
* eating disorder
* displaying acutely suicidal behaviors
15 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of California, San Diego
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jyoti Mishra
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jyoti Mishra, PhD
Role: PRINCIPAL_INVESTIGATOR
University of California, San Diego
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UC San Diego Health Psychiatry
San Diego, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PERMA
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.