Mindfulness-based Intervention to Address PTSD in Trauma-exposed, Homeless Women

Sponsor
University of California, Irvine (Other)
Overall Status
Recruiting
CT.gov ID
NCT04605198
Collaborator
(none)
134
2
2
22.8
67
2.9

Study Details

Study Description

Brief Summary

Posttraumatic stress disorder (PTSD) is a major public health concern that disproportionately effects minorities and those with low-socioeconomic status, such as homeless women, creating a critical health disparity. PTSD has been linked with dysregulated hypothalamic-pituitary-adrenal (HPA) functioning and increased inflammation, which can lead to long-term physical-health problems and PTSD-symptom maintenance, exacerbating disparities. Mindfulness-based interventions, including Mindfulness-based Stress Reduction (MBSR), have shown promise as a complementary tool for addressing PTSD in veterans and with low-income, minority populations, but homeless women have not been examined adequately. MBSR may improve PTSD symptomatology and help modulate the dysregulated stress response common in individuals with PTSD, improving physical and mental health concurrently. This project is an open-label, parallel, modified-cross over clinical trial of a modified-MBSR intervention to reduce PTSD symptoms in homeless women and to explore physiological correlates of treatment-response.

Hypotheses:
  1. Participation in an MBSR-based intervention will be associated with clinically significant reduction in PTSD (primary outcome), lower depression symptoms and greater drug and alcohol abstinence (secondary outcomes) compared to participation in an attention control.

  2. Compared to an attention control, participants in an MBSR-based intervention group will demonstrate improvements in cortisol reactivity and lower inflammation.

At baseline, women will complete psychosocial assessments (e.g., depression, substance use, trauma history) and participate in a brief stress task, providing salivary samples before and after the task (which will be assayed for cortisol and C-reactive protein, a marker of inflammation). Women will then participate in 1) a 9-session MBSR-based program that was modified based on an initial qualitative component that involved a Community Advisory Board and focus groups with women from the community (N=4 focus groups; 28 women total) or 2) a nine-session health-promotion course (i.e., attention-control condition). Follow-up assessments that include psychosocial and biological data will occur immediately after final intervention session and again 6-months later. Clinically-meaningful improvements in PTSD (primary outcome) and secondary outcomes (e.g., depression, substance use, inflammation, cortisol reactivity) will be examined.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Modified Mindfulness-based Stress Reduction
  • Behavioral: Health Promotion Wellness Classes
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
134 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be recruited from two sites. To avoid contamination between subjects living at the sites, using a quasi-randomized method, all participants at each site will receive the same treatment per cohort. Sites will alternate between the assignment of treatment (modified-MBSR) or control (health promotion class) in sequential cohorts to account for between site differences.Participants will be recruited from two sites. To avoid contamination between subjects living at the sites, using a quasi-randomized method, all participants at each site will receive the same treatment per cohort. Sites will alternate between the assignment of treatment (modified-MBSR) or control (health promotion class) in sequential cohorts to account for between site differences.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Mindfulness-based Intervention to Address PTSD in Trauma-exposed, Homeless Women
Actual Study Start Date :
Oct 6, 2020
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Modified Mindfulness-based Stress Reduction

Behavioral: Modified Mindfulness-based Stress Reduction
Participants will be trained in mindfulness meditation and the applicability of mindfulness practices to daily life. During MBSR programming, teachers will lecture about key topics in mindfulness and lead class discussions. Participants are given homework assignments, such as listening to guided meditations. Participants are given opportunities to ask the instructor questions and to share their experiences with each other. Each session focuses on a different key topic. Topics are: Session 1: Introduction; Session 2: Understanding Perceptions; Session 3: Hatha Yoga, Sitting Meditation, Walking Meditation; Session 4: Concentration & Awareness; Session 5: Unhealthy Patterns &Getting Unstuck; Session 6: Transformational Coping Strategies; Session 7: Mini-retreat; Session 8: Maintaining Discipline & Flexibility; Session 9: Course Review.
Other Names:
  • modified MBSR
  • Active Comparator: Health Promotion Attention Control

    Behavioral: Health Promotion Wellness Classes
    Sessions will cover the following general wellness topics: Session 1; Introduction; Session 2: Envisioning Health Through Art; Session 3: Chronic Disease 1 (Heart Health); Session 4: Chronic Disease II (Diabetes); Session 5: Nutrition and Hydration; Session 6: Infectious Disease Prevention; Session 7: Skin Care; Session 8: Oral Health; Session 9: Promoting Social Integration & Course Graduation.

    Outcome Measures

    Primary Outcome Measures

    1. Post-traumatic Stress Symptoms [Immediately post-intervention & 6-month follow-up]

      Clinically significant improvement in Posttraumatic Stress Symptoms - PTS (i.e., decrease in symptoms), as measured by the PTSD Checklist for DSM 5 (PCL-5) (DSM=Diagnostic and Statistical Manuel of Mental Disorders). The PCL-5 is a 20-item scale (range 0-80), with rating scale descriptions: 0 "Not at all," 1 "A little bit," 2 "Moderately," 3 "Quite a bit," and 4 "Extremely." Higher scores indicate more PTSD symptoms.

    Secondary Outcome Measures

    1. Depression [Immediately post-intervention & 6-month follow-up]

      Change in depressive symptoms from baseline to follow-ups (i.e., decrease in symptoms), using the Patient Reported Outcomes Measurement Information System (PROMIS) measure for depression. The PROMIS asks 9-items (range 9-45) with response options: 1 "never", 2 "rarely", 3 "sometimes", 4 "often", and 5 "always". Higher scores indicate more symptoms of depression.

    2. Substance Use (self-report) [Immediately post-intervention & 6-month follow-up]

      Change in substance use from baseline to follow-ups using the Texas Christian University Screen

    3. Substance Use (objective) [Immediately post-intervention & 6-month follow-up]

      Change in substance use from baseline to follow-up using 5-panel FDA-approved urine test cup

    4. Cortisol reactivity [Immediately post-intervention & 6-month follow-up]

      Change in cortisol reactivity using script driven imagery from baseline to follow-up using standard manufacturer protocols (from Salimetrics).

    5. C-Reactive Protein (CRP) [Immediately post-intervention & 6-month follow-up]

      Change in CRP, measured via saliva using the Salivary C-Reactive Protein ELISA kit, an enzyme-linked immunoassay.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. self-reported homeless women

    2. age 18-64

    3. willing to provide informed consent

    4. lifetime exposure to at least one DSM-V qualifying trauma

    5. likely subthreshold or threshold PTSD, as measured by the PCL-5.

    Note: A homeless person is defined as anyone who spent the previous night in a public or private shelter, or on the street.

    Exclusion Criteria:
    1. not speaking English

    2. judged to be cognitively impaired; as indicated by score >9 on the Short-Blessed Screener (SBS).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 North County Serenity House Escondido California United States 92026
    2 Prototypes Women's Center Pomona California United States 91767

    Sponsors and Collaborators

    • University of California, Irvine

    Investigators

    None specified.

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Dana Rose Garfin, Assistant Adjunct Professor, University of California, Irvine
    ClinicalTrials.gov Identifier:
    NCT04605198
    Other Study ID Numbers:
    • MD013910-01 [HS# 2019-5607]
    First Posted:
    Oct 27, 2020
    Last Update Posted:
    Apr 20, 2021
    Last Verified:
    Apr 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Dana Rose Garfin, Assistant Adjunct Professor, University of California, Irvine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 20, 2021