Actively Recruiting
Women's Wellbeing Study
Led by Butler Hospital · Updated on 2025-09-26
48
Participants Needed
1
Research Sites
91 weeks
Total Duration
On this page
Sponsors
B
Butler Hospital
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Phase 2 is a randomized controlled trial of integrative yoga and mindful self-compassion program vs. women's wellbeing education for women with a history of interpersonal violence exposure and heightened distress.
CONDITIONS
Official Title
Women's Wellbeing Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female
- Aged 18 to 65 years
- Experienced interpersonal violence at any point in life, confirmed by Trauma History Questionnaire
- Currently distressed with a score greater than 5 on the Kessler-6 screener
- Speak and understand English well enough to understand questionnaires when read aloud
- Have access to a telephone
- Have access to a device that supports video platform use for assessments and home yoga sessions
You will not qualify if you...
- Unable to be physically active based on Physical Activity Readiness Questionnaire score and physician consent
- Planned surgery within the next 6 months
- Currently pregnant
- Current mania as assessed by DIAMOND
- Lifetime history of psychotic disorders (DIAMOND)
- Current probable severe substance use disorder (DIAMOND)
- Current or recent (past year) diagnosis of anorexia nervosa (DIAMOND)
- Moderate or high suicide risk or recent suicidal plan/intent
- Unstable psychiatric treatments in past 8 weeks
- Planning to move away within 6 months
- Experiencing intimate partner violence currently or within past 6 months
- Currently practicing yoga weekly or involved in mindfulness-based programs
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Butler Hospital
Providence, Rhode Island, United States, 02906
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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