IFS for BPDInternal Family Systems Therapy for Borderline Personality Disorder Symptom Improvement
This study aims to evaluate the effectiveness of Internal Family Systems Therapy in improving symptoms associated with Borderline Personality Disorder.
Internal family systems therapy
Mental Disorders
+ Borderline Personality Disorder
+ Personality Disorders
Treatment Study
Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.Borderline Personality Disorder (BPD) is a mental health condition that causes emotional instability, identity issues, relationship problems, and impulsive behavior. It affects a significant number of people, contributing to high healthcare usage, suicide risk, and long-term disability. Current therapies show some benefits, but they are limited and resource-intensive. This study aims to evaluate the effectiveness of Internal Family Systems (IFS) therapy in improving mental health in individuals with BPD. IFS therapy targets core issues of BPD such as emotional instability, shame, and self-fragmentation. The study hypothesizes that participants will show noticeable improvements in BPD symptoms and overall well-being. The study will recruit fifteen adults with a formal BPD diagnosis. Participants will receive weekly, one-hour IFS therapy sessions over approximately 12 to 15 months. The therapy will be delivered by licensed mental health professionals trained in the IFS model. Participants will pay a reduced fee for the sessions. The study will measure BPD symptom severity as the primary outcome, and secondary outcomes include changes in emotional instability, shame, self-compassion, relationship functioning, depression, anxiety, addictive behaviors, and overall well-being. Feasibility, acceptability, and safety of the therapy will also be evaluated. Data will be collected electronically and analyzed using statistical methods. The study is set to begin in early 2026 and conclude by the end of 2027, with data analysis and results dissemination planned for 2028.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.15 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Resident of Ontario, Canada; * Sufficient fluency in English to provide informed consent, participate in therapy sessions, and complete self-reported assessments; * Diagnosis of borderline personality disorder confirmed by a healthcare professional authorized to establish such a diagnosis in Ontario; * Willingness and ability (including financial means) to participate in the 50-session, 12-15-month intervention and the study assessments; * Capacity and willingness to provide written informed consent. Exclusion Criteria: * Current manic or psychotic symptoms regardless of diagnosis; * Substance dependence severe enough to interfere with meaningful level of engagement in the study intervention. * Cognitive impairment or neurological disorders that would preclude informed consent or meaningful participation in the study intervention. * Concurrent participation in any another form of psychotherapy.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Provincewide across Ontario (intervention can be delivered virtually)
Tiny, CanadaOpen Provincewide across Ontario (intervention can be delivered virtually) in Google Maps