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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06185959
Other study ID # 72936
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 1, 2024
Est. completion date June 1, 2027

Study information

Verified date April 2024
Source Stanford University
Contact Lisa Zhang, PhD
Phone 650-721-8590
Email lisaz@stanford.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study's overarching aim is to evaluate a new psychoeducation and process group for Asian and Asian American psychiatric outpatients. This is a 12 week mental health group which will focus on both educational content related to Asian mental health as well as increasing connection between group members. We hypothesize that participants in the group will experience a decrease in psychiatric symptoms at the conclusion of the group compared to their symptoms at the beginning of group. We also hypothesize that participants will feel more socially connected after the group.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date June 1, 2027
Est. primary completion date June 1, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years and older - Participants must identify as Asian or Asian American - Sufficient English proficiency to participate in a psychotherapy group conducted in English Exclusion Criteria: - Unable to provide written informed consent - Elevated suicide risk (e.g. recent active suicidal ideation, past-year suicide attempt) without a current individual mental health provider - Any other challenges that would preclude participation in group psychotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Psychoeducation and Process Group for Asian and Asian American Psychiatric Outpatients
Participants will be individuals enrolling in a 1.5 hour weekly therapy group lasting 12 weeks and will be invited to participate in research on group processes and outcomes. The psychoeducation and process group will be a 12-session weekly closed group with 10-15 participants per group (2-3 groups total) conducted via Zoom to enhance accessibility and reduce barriers to care. Groups will be co-led by licensed clinical psychologists with experience providing both group psychotherapy and culturally responsive services. Group sessions will include brief check-ins, collaborative agenda-setting, a mini-didactic, individual reflection, and group discussion. The didactics curriculum will include topics such as intergenerational trauma, cultural differences in emotional expression, the model minority myth, family dynamics, racism, and positive connections to culture.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Health Questionnaire-9 (PHQ-9) Depression symptoms assessed on 4-point Likert scale. Score range from 0 to 27, with higher scores representing more severe depression symptoms Once at baseline, once at 6 weeks, once at 12 weeks
Primary Generalized Anxiety Disorder Screener-7 (GAD-7) Anxiety symptoms assessed on 4-point Likert scale. Score range from 0 to 21, with higher scores representing more severe anxiety symptoms Once at baseline, once at 6 weeks, once at 12 weeks
Secondary Social Connectedness Scale Subjective social connectedness assessed on 6-point Likert scale. Score range from 20 to 120, with higher scores representing higher perceived social connectedness Once at baseline, once at 12 weeks
Secondary Rosenberg Self-Esteem Scale Subjective self-esteem assessed on 4-point Likert scale. Score range from 10 to 40, with higher scores representing higher self-esteem Once at baseline, once at 12 weeks
Secondary Self-Stigma of Seeking Help Scale Help-seeking self-stigma assessed on 5-point Likert scale. Score range from 10 to 50, with higher scores representing higher self-stigma of seeking help Once at baseline, once at 12 weeks
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