Actively Recruiting
Photo-experiencing and Reflective Listening (PEARL) to Promote Healing Engagement for Survivors of Violence
Led by Temple University · Updated on 2025-12-23
40
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
Sponsors
T
Temple University
Lead Sponsor
N
National Institute of Nursing Research (NINR)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if a photo-elicitation intervention called PEARL (Photo-experiencing and Reflective Listening) can promote healing engagement in survivors of interpersonal violence. It will also learn about the feasibility and acceptability of PEARL. The main questions it aims to answer are: Does PEARL reduce barriers to help-seeking for trauma? Does PEARL improve trauma coping self-efficacy? Does PEARL change post-trauma cognitions and readiness for recovery? Is PEARL feasible and acceptable to survivors of interpersonal violence? Researchers will compare people who receive PEARL immediately to people on a waitlist (who receive PEARL three months later) to see if PEARL improves healing engagement and help-seeking behaviors. Participants will: * Complete baseline surveys about their trauma history, mental health, healing, and help-seeking behaviors * Be randomly assigned to receive PEARL immediately or after a 3-month wait * Receive a photography-focusing prompt and create photos over two weeks (those in the immediate group or after the waiting period) * Participate in a reflective listening interview about their photos * Complete follow-up surveys immediately after the intervention and one month later * Participate in a one-month follow-up interview about their experience
CONDITIONS
Official Title
Photo-experiencing and Reflective Listening (PEARL) to Promote Healing Engagement for Survivors of Violence
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Identifies as a survivor of interpersonal violence
- Able to complete an interview in English
- Able to provide informed consent
You will not qualify if you...
- Under 18 years of age
- Does not identify as a woman
- No history of interpersonal violence
- Unable to complete an interview in English
- Unable to provide informed consent
AI-Screening
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Trial Site Locations
Total: 1 location
1
Women in Transition
Philadelphia, Pennsylvania, United States, 19122
Actively Recruiting
Research Team
L
Laura M Sinko, PhD, MSHP, RN
CONTACT
K
Kayleigh Izzo, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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