- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03414606
Social Behavior in Depression (HLGDep)
February 4, 2018 updated by: ma, yina, Beijing Normal University
In the project, investigators basically plan to test the difference in social behavior and social cognition between depressive patients and healthy individuals.
To test this, investigators plan to use traditional or novel behavioral experiment paradigms to target various behaviors.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
25
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yina Ma, Doctor
- Phone Number: +8613810258647
- Email: yma@bnu.edu.cn
Study Locations
-
-
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Beijing, China
- Recruiting
- HuiLongGuan Hospital
-
Contact:
- Yina Ma, Doctor
-
Principal Investigator:
- Yina Ma, Doctor
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Individuals diagnosed with depression and healthy control
Description
Inclusion Criteria:
- Age range between 18 and 60
- Education experience above high school
- Score for Hamilton's Depression Scale >=17
- Diagnosis of depression through Scid
Exclusion Criteria:
- Undergoing electric shock treatment in 3 months
- Excluding those who with bipolar disorder
- Excluding those who with postpartum depression
- Excluding those who with hysteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prosocial behavior
Time Frame: Baseline
|
The prosocial behavior will be assessed by conventional economic games, including dictator game, message game, and ultimatum game.
|
Baseline
|
Cognitive flexibility
Time Frame: Baseline
|
Cognitive flexibility will be assessed by psychological cognitive paradigm, i.e. reversal learning paradigm.
The participants will be asked to choose the item with high probability to win reward.
|
Baseline
|
Valuation of social information
Time Frame: Baseline
|
The valuation of social information was measured by psychological paradigm, developed from animal studies, called "pay-per-view".
The participants will be asked make decision about more social information or more monetary reward.
|
Baseline
|
Optimism bias
Time Frame: Baseline
|
Participants will complete two sessions of life event estimation, i.e. estimating their likelihood of experiencing each event on a self-paced basis.
|
Baseline
|
Emotion recognition
Time Frame: Baseline
|
After viewing a video, participants will be asked to judge the person's attitude in the video.
Through this paradigm, investigators could test emotional bias in social interaction in depressive patients.
|
Baseline
|
Model-free & model-based tendency
Time Frame: Baseline
|
Participants will be asked to complete a two-stage task, by choosing the stimuli with high probability to obtain reward.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Yina Ma, Doctor, Beijing Normal University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2017
Primary Completion (Anticipated)
February 16, 2018
Study Completion (Anticipated)
March 1, 2018
Study Registration Dates
First Submitted
January 22, 2018
First Submitted That Met QC Criteria
January 26, 2018
First Posted (Actual)
January 30, 2018
Study Record Updates
Last Update Posted (Actual)
February 6, 2018
Last Update Submitted That Met QC Criteria
February 4, 2018
Last Verified
February 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HLGdepression
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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