Interchangeability of the Working Alliance Inventory and Working Alliance Inventory, Short Form.
Michael A Busseri, John D Tyler
https://pubmed.ncbi.nlm.nih.gov/12847779/Actively Recruiting
Led by University of Social Sciences and Humanities, Warsaw · Updated on 2025-09-24
80
Participants Needed
1
Research Sites
4 weeks
Total Duration
This research aims to explore the use of generative artificial intelligence to create personalized therapeutic scripts for imagery rescripting ImRs based on participants childhood memories of parental criticism and neutral events. The study focuses on evaluating emotional and physiological responses to AI-generated content and compares the effects of an ImRs intervention with no therapeutic modification. The trial involves adults aged 18 to 35 with generalized anxiety, fear of failure, and rumination symptoms. Participants will provide descriptions of two critical and two neutral childhood memories, which will be used to generate personalized scripts with the Gemini large language model. On Day 1, all participants will listen to both critical and neutral scenarios. They will be randomly assigned to either an experimental group receiving an ImRs intervention, where a therapist figure addresses unmet needs in the critical memory script, or a control group hearing the unmodified scripts. Skin conductance and emotional ratings will be recorded during the session. Follow-up questionnaires will be completed one week later. During the study, participants will rate their emotional responses, and physiological arousal will be monitored continuously. Licensed cognitive-behavioral therapists will evaluate the therapeutic quality of the generated scripts. Outcome measures include anxiety symptoms, intrusive thoughts, emotional intensity, and physiological responses to the scenarios. The study will assess the feasibility of AI-assisted therapeutic scripts and their potential to reduce distress and improve emotional regulation over time.
CONDITIONS
Optimization of Imagery Rescripting Research Using Generative Artificial Intelligence
S
Stanisław Karkosz, MA
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University of Social Sciences and Humanities, Warsaw
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants listen to personalized audio scripts based on their own childhood memories of parental criticism and neutral events during a laboratory session. The experimental group hears a modified critical scenario with an imagery rescripting intervention, while the control group hears unmodified scenarios. Emotional responses are rated and skin conductance is recorded throughout the session.
1 visit (in-person)
Duration - 1 day (1 week after treatment)
One week after the laboratory session, participants complete questionnaires assessing generalized anxiety and frequency of intrusive thoughts related to their memories.
1 follow-up visit (remote or in-person)
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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Lead Sponsor