RECRUITING

Single Session Intervention to Promote Hope

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to develop a brief, self-guided single-session intervention (SSI) that targets the development of, or increase in, hope, and pilot test it for the primary outcomes of feasibility, acceptability/likeability, safety, and changes in hope, and the secondary outcomes of self-worth, empowerment, and emotional wellbeing among women experiencing intimate partner violence (IPV). The study will be conducted in 2 stages: intervention development (Intervention Development Stage), and pilot testing the intervention (Pilot Stage). The focus of this registration is the Pilot Stage.

Official Title

Hope as a Path to Healing: Developing a Single-Session Intervention for Women Who Experience Intimate Partner Violence

Quick Facts

Study Start:2024-05-07
Study Completion:2025-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06375876

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-identify as a woman (cis- or trans-gender woman)
  2. * Currently in a relationship of at least 3 months duration in which they have experienced physical IPV by a male partner
  3. * Have a smartphone that is compatible with the MyCap app to be able to participate in daily surveys.
  1. * Have experienced significant psychiatric instability based on self-reported inpatient psychiatric hospitalization in the past 3 months
  2. * Reports having a conservator of person
  3. * Not comfortable conversing, reading, or writing in English
  4. * Participated in a Listening Session in the development phase of this study.

Contacts and Locations

Study Contact

Tami Sullivan, PhD
CONTACT
203-789-7645
tami.sullivan@yale.edu
Ashley Clayton, MA
CONTACT
203-623-9830
ashley.clayton@yale.edu

Principal Investigator

Tami Sullivan, PhD
PRINCIPAL_INVESTIGATOR
Department of Psychiatry, Yale School of Medicine

Study Locations (Sites)

The Consultation Center at Yale
New Haven, Connecticut, 06511
United States

Collaborators and Investigators

Sponsor: Yale University

  • Tami Sullivan, PhD, PRINCIPAL_INVESTIGATOR, Department of Psychiatry, Yale School of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-07
Study Completion Date2025-04

Study Record Updates

Study Start Date2024-05-07
Study Completion Date2025-04

Terms related to this study

Keywords Provided by Researchers

  • Intimate Partner Violence (IPV)

Additional Relevant MeSH Terms

  • Domestic Violence