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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05930886
Other study ID # 00024335
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 15, 2023
Est. completion date June 30, 2024

Study information

Verified date May 2024
Source Oregon Health and Science University
Contact Jeanette Johnstone, PhD
Phone 503-494-3700
Email jojeanet@ohsu.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Focus groups to identify treatment needs and barriers to participation in the planned multinutrient study among racially and ethnically diverse (Black and Hispanic) communities.


Description:

Focus group purpose is to understand parents' priorities regarding their child's mental health, and facilitators or barriers to research participation generally, with inquiry about CIH intervention use, and the multinutrient feasibility study specifically. Researchers will engage Black and Hispanic families in focus groups to discuss mental health priorities related to their children, and real or perceived barriers to engagement in research studies. The feedback will inform the final design and recruitment for the multinutrient feasibility study in Black and Hispanic populations. One group will comprise individuals who self-identify as Hispanic, another, as Black, in order to create space to hear perspectives that may differ between broadly defined groups.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date June 30, 2024
Est. primary completion date May 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Adult parents/caregivers self-identified as Black or Hispanic/Latino - With a family member 6-18 years old with suspected ADHD and/or emotional dysregulation, or provide care for, or teach someone who meets these criteria - Who have sought or are interested in treatment - Willing to discuss child's mental health care needs and provide feedback regarding feasibility study - Able to attend focus groups in person - Able to communicate in English or Spanish - Agree to focus group session audio recording Exclusion Criteria: - Unwilling to be recorded

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Focus Group
Black or Hispanic/Latino parents, caregivers or family members of children with ADHD symptoms and/or emotional dysregulation, will discuss: (1) impact of child's mental health, treatments, care received; (2) perceived and actual barriers to future study participation, including discussion about acceptability of bio-specimen collection methods for urine and blood. Each group will comprise individuals who self-identify as Hispanic/Latino, Black, or mixed race. Groups are anticipated to comprise individuals who identify with one or the the other race/ethnicity in order to create space to hear perspectives that may differ between these broadly defined groups.

Locations

Country Name City State
United States Oregon Health & Science University Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Input and Feedback on Proposed Feasibility Study Purpose is understanding
Parents' priorities regarding their child's mental health
Facilitators or barriers to research participation generally
Parent input on planned study specifically
Specific recommendations for modifying the future feasibility study design
Previous CIH intervention use
Baseline
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