Clinical Trial

Imagery Rescripting for Pathological Affective Dependence and Intimate Partner Violence

Study acronym: ImRs-PAD
Not Yet Recruiting
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Record status
This record was last updated November 1, 2024 (before its estimated May 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this multiple baseline case series study is to evaluate the effectiveness of Imagery Rescripting for Pathological Affective Dependence (PAD) in victims of Intimate Partner Violence (IPV). The primary research questions are: Does Imagery Rescripting reduce PAD and/or commitment to the abusive relationship after separation? Does Imagery Rescripting also reduce traumatic symptoms? Does Imagery Rescripting improve general mental health, self-compassion, and resilience in IPV victims? Participants will undergo a waiting period of 5-9 weeks (to assess time effects without treatment), followed by 4 weekly preparation sessions, 12 weekly Imagery Rescripting sessions, and 1 month of post-treatment. Throughout the study, participants will rate the severity of PAD and relational commitment on a weekly basis. They will also complete more detailed questionnaires assessing mental health, traumatic symptoms, resilience, and self-compassion before each phase, at 1 month post-treatment, 3 months post-treatment, and during follow-ups at 6 and 12 months.
Trial Details
NCT Number NCT06670326
Lead Sponsor University of Amsterdam
Collaborators: VU University of Amsterdam, Stichting Achmea Slachtoffer en Samenleving
Conditions Pathological Affective Dependence
Enrollment 18 participants
Start Date 2025-02-01
Primary Completion 2025-05 (estimated)
Study Completion 2026-02 (estimated)
Updated on ClinicalTrials.gov 2024-11-01