Treatments for Improving Mood in Women Survivors of Interpersonal Violence: A Community-Engaged Study-1.2

Description

Phase 1.2: Open Trial N=15 women survivors of interpersonal violence will be enrolled into a single-arm pilot trial to test the adapted integrative hatha yoga and mindful self-compassion program.

Conditions

Distress

Study Overview

Study Details

Study overview

Phase 1.2: Open Trial N=15 women survivors of interpersonal violence will be enrolled into a single-arm pilot trial to test the adapted integrative hatha yoga and mindful self-compassion program.

Adaptation and Pilot Study of Integrative Yoga and Mindful Self-Compassion (I-YMSC) to Improve Mood in Women Survivors of Interpersonal Violence

Treatments for Improving Mood in Women Survivors of Interpersonal Violence: A Community-Engaged Study-1.2

Condition
Distress
Intervention / Treatment

-

Contacts and Locations

Providence

Butler Hospital, Providence, Rhode Island, United States, 06442

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Female
  • 2. Ages 18-65
  • 3. Self-identify as Black/African American, Hispanic/Latino(e/x), or White
  • 4. Report having experienced interpersonal violence (defined to include all forms throughout the lifespan, confirmed with the Trauma History Questionnaire (THQ\])
  • 5. Report being distressed, defined by a score of \>5 on the Kessler-6 screener
  • 6. Speak and understand English well enough to understand questionnaires when they are read aloud
  • 7. Have access to a telephone through owning one, a relative/friend, or an agency
  • 8. Have access to a device that will support use of the video platform we are using to conduct assessments and for home practice yoga video sessions
  • 1. Inability to be physically active, determined by a score \>1 on the Physical Activity Readiness Questionnaire (PAR-Q) and physician non-consent of participation
  • 2. Planned surgery in next 6 months, as this would interfere with study participation
  • 3. Pregnancy, as yoga should be modified for pregnancy
  • 4. Current mania as determined by the Diagnostic Interview for Anxiety, Mood, and OCD and Related Neuropsychiatric Disorders (DIAMOND)
  • 5. Lifetime history of psychotic disorders (DIAMOND)
  • 6. Current probable severe substance use disorder (DIAMOND)
  • 7. Current diagnosis of anorexia nervosa or history in past year (DIAMOND)
  • 8. Moderate or high risk for suicide on the adapted Columbia Suicide Severity Rating Scale screen version-recent (C-SSRS) and/or endorsement of suicidal plan/intent in the past 3 months
  • 9. Non-stable course of psychiatric treatments (medication, psychotherapy) for the last 8 weeks
  • 10. Plan to move from the area in the next 6 months, as this may preclude study participation given enrollment timeframes
  • 11. Self-report of experiencing intimate partner violence currently or within past six months (assessed by the Revised Conflict Tactics Scale 2 \[R-CTS2\]), as this would require a different type of intervention
  • 12. Current weekly yoga practice or current participation in mindfulness-based programming, as these are the study interventions

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Butler Hospital,

Study Record Dates

2025-09