Correlation Between Psychological Resilience and Genetic, Inflammatory Indicators
A Study of the Correlation Between Psychological Resilience and Genetic, Inflammatory Indicators in Young Population
1 other identifier
observational
400
0 countries
N/A
Brief Summary
The goal of this observational study is to evaluate and analyze the influencing factors of the adaptive ability of young people, explore the impact of the interaction of environment and gene on the psychological adaptive ability of young people, incorporate the prediction model of the dynamic change of adaptive ability, build a standardized norm of young people's adaptive ability, and form a grading reference standard system. The main questions it aims to answer are:
- What are most important influencing factors for the adaptive ability of young people?
- How the environment and gene interact with each other on the psychological adaptive ability of young people?
- Can we build a prediction model of the dynamic change of adaptive ability and form a grading reference standard system? Participants will support us with basic information data, adaptive ability assessment data, genetic testing data, brain image scanning data, and inflammatory indicators data. Then subjects were divided into very low adaptive group, low adaptive group, high adaptive group and very high adaptive group according to the quartile of adaptive ability score. And the statistical analysis will be performed by the data analyst.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 11, 2023
CompletedStudy Start
First participant enrolled
January 1, 2024
CompletedFirst Posted
Study publicly available on registry
January 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedJanuary 5, 2024
December 1, 2023
3 months
December 11, 2023
December 21, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
the Assessment of the Psychological Resillience
Psychological Resillience was evaluated across multiple dimensions, including cognitive functioning, stress coping, psychological well-being, and personality traits, and was measured using internationally accepted scales. Psychological Resillience is measured using the Psychological Resilience Scale (CD-RISC), which consists of 25 items rated on a 5-point Richter's scale, with scores ranging from 0 to 4 indicating that this is not the case at all, seldom the case, sometimes the case, often the case, and almost always the case. The sum of the scores of the items is the total score of the scale, and the total score is 0\~100, the larger the score indicates the higher the level of psychological resilience, and the score of less than 60 is the poor level of psychological resilience, 61\~69 is the average level of psychological resilience, 70\~79 is the good level of psychological resilience, and \>=80 is the excellent level of psychological resilience.
1 year
Study Arms (4)
very low adaptive group
The subjects were divided into very low adaptive group, low adaptive group, high adaptive group and very high adaptive group according to the quartile of adaptive ability score.
low adaptive group
The subjects were divided into very low adaptive group, low adaptive group, high adaptive group and very high adaptive group according to the quartile of adaptive ability score.
high adaptive group
The subjects were divided into very low adaptive group, low adaptive group, high adaptive group and very high adaptive group according to the quartile of adaptive ability score.
very high adaptive group
The subjects were divided into very low adaptive group, low adaptive group, high adaptive group and very high adaptive group according to the quartile of adaptive ability score.
Interventions
no intervention
Eligibility Criteria
18-24 years old young people
You may qualify if:
- Age 18-24 years old; high school graduation and above; agree to collect blood samples and sign an informed consent form.
You may not qualify if:
- Did not consent to the collection of blood samples; did not sign an informed consent form; suffered from a major illness such as a malignant tumor.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Greenberg RL, Guzick AG, Schneider SC, Weinzimmer SA, Kook M, Perozo Garcia AB, Storch EA. Depressive Symptoms in Autistic Youth with Anxiety Disorders. J Dev Behav Pediatr. 2023 Dec 1;44(9):e597-e603. doi: 10.1097/DBP.0000000000001223. Epub 2023 Oct 11.
PMID: 38019467BACKGROUNDBrunette MF, Erlich MD, Edwards ML, Adler DA, Berlant J, Dixon L, First MB, Oslin DW, Siris SG, Talley RM. Addressing the Increasing Mental Health Distress and Mental Illness Among Young Adults in the United States. J Nerv Ment Dis. 2023 Dec 1;211(12):961-967. doi: 10.1097/NMD.0000000000001734.
PMID: 38015186BACKGROUNDWong WLE, Arathimos R, Lewis CM, Young AH, Dawe GS. Investigating the role of the relaxin-3/RXFP3 system in neuropsychiatric disorders and metabolic phenotypes: A candidate gene approach. PLoS One. 2023 Nov 15;18(11):e0294045. doi: 10.1371/journal.pone.0294045. eCollection 2023.
PMID: 37967073BACKGROUND
Biospecimen
Form of biological specimen storage: venous blood was collected on an empty stomach, 5 ml was placed in a blood collection tube containing procoagulant and 5 ml was placed in a blood collection tube containing anticoagulant. Blood and other non-tissue samples are stored in a refrigerator at -86°C. The identification of the stored samples is unique and does not contain any donor identification information; the unique code is automatically and randomly generated by the sample bank management system and consists of 18 digits.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Guang Zhang, Dr
Qianfoshan Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Vice President
Study Record Dates
First Submitted
December 11, 2023
First Posted
January 5, 2024
Study Start
January 1, 2024
Primary Completion
March 31, 2024
Study Completion
December 31, 2024
Last Updated
January 5, 2024
Record last verified: 2023-12
Data Sharing
- IPD Sharing
- Will not share
There is not a plan to make IPD available.