Culturally Tailored ACT for Black Trauma

Not Applicable

Withdrawn

• Conditions: Stress Disorders, Traumatic; Anxiety; Anxiety Disorders
• Interventions: Behavioral: Classic ACT program; Behavioral: POOF ACT program

• Registration Number: NCT06296030
• Lead Sponsor: Azusa Pacific University

Brief Summary

Blacks in America more frequently meet the criteria for posttraumatic stress disorder (PTSD) than any other US race or ethnicity. Yet, blacks are among the groups least likely to use mental health services for trauma. Thus, a large number of traumatized blacks suffer silently and remain untreated.

Acceptance and Commitment Therapy (ACT) is an empirically-based psychological intervention that uses acceptance and mindfulness strategies, with commitment and behavior change strategies, to increase psychological flexibility and decrease anxiety outcomes. While culturally tailored mental health interventions have been shown useful for racial and ethnic minorities, there have been few efforts to tailor ACT for blacks. This NIH R21 would compare an ACT model specifically culturally tailored for blacks (POOF) to the classic ACT model in a randomized trial, where clinicians will conduct 12-session telehealth synchronous virtual groups. Eighty black participants who self-identify as suffering from stress or anxiety will be confidentially recruited. Two specific aims are proposed:

Aim 1) It is expected that POOF participants will report higher levels of acceptability of treatment than classic ACT participants and that POOF participants will have better adherence to treatment regimens than traditional ACT participants.

Aim 2) Given that race-based stress may mediate anxiety symptoms in U.S. based blacks, it is expected that POOF will decrease race-based stress, thereby mattering the most for improving anxiety outcomes for blacks.

The proposed R21 pilot study will be the first randomized controlled trial to evaluate an ACT intervention tailored explicitly for black racial trauma. This study will provide critical data needed to plan and design a future R01 controlled longitudinal effectiveness study. The long-term objective is to significantly reduce the prevalence of stress and anxiety-related symptoms due to traumatic events for Blacks by increasing treatment acceptability for this population. Since blacks have the highest rates of trauma prevalence and chronicity, yet they are still underrepresented in mental health treatment, this tailored intervention can have a significant public health impact.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-02-05
• Study Start: 2021-09-01
• Primary Completion: 2022-09-01
• Study Completion: 2023-08-31
• Status Verified: 2024-02
• Study First Submitted QC: 2024-02-28
• Last Update Submitted: 2024-02-28
• Study First Posted: 2024-03-06
• Last Update Posted: 2024-03-06

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• willing/ desiring to commit to engagement in a 12-week tele-health anxiety group
• self-identifies as African American or of Black American heritage
• age 18 years or over
• age 65 years or younger
• English-speaking, writing, and understanding
• able to provide informed consent
• is experiencing mild or moderate anxiety or stress-related symptoms, based on pre-screening testing
• has experience with video-based social media, Zoom, or other synchronous video-based modalities

Exclusion Criteria

• At the screening, those who state they have additional psychological, behavioral, or medical disorders (outside of anxiety, stress, or trauma-related disorders) as their primary concern. For instance, if a participant was diagnosed with major depressive disorder as primary and an anxiety disorder as secondary, they would be excluded from the study.
• At the screening, those who are experiencing anxiety due to a physical condition (due to a cancer diagnosis or some other physical diagnosis) would be excluded from this study.
• Individuals who are experiencing extreme psychological symptoms are not appropriate for a tele-health group format.
• Persons who are on medication for any psychological disorder at the time of screening may not be appropriate for this tele-health group format.
• Those who have not been introduced to web-based formats of live interaction prior to the study (if they have no experience with technology or they are not comfortable with technology) would not be appropriate for this particular tele-health pilot study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Arm && Interventions

Group	Intervention	Description
Classic ACT program	Classic ACT program	Participants will engage in pre-test measures (anxiety, race-based stress, and psychological flexibility). Subjects will then participate in a 12-week telehealth group (once a week, 2 hours a week) with other group members where a classic Acceptance and Commitment Therapy protocol will be administered. After this, participants will engage in post-test measures.
POOF ACT program	POOF ACT program	Participants will engage in pre-test measures (anxiety, race-based stress, and psychological flexibility). Subjects will then participate in a 12-week telehealth group (once a week, 2 hours a week) with other group members where an Acceptance and Commitment Therapy protocol will be administered that has been culturally tailored to address African American racial trauma. After this, participants will engage in post-test measures.

Primary Outcome Measures

Name	Time	Method
Race-Based Traumatic Stress	12-weeks	The Race-Based Traumatic Stress Symptom Scale (RBTSSS)

Trial Locations

Locations (1)

Azusa Pacific University; 🇺🇸 Azusa, California, United States