Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06699732

Impact of Mindful Self-Compassion Therapy on Self Harm Behaviors, Emotional Regulation and Quality of Life Among Patients With Borderline Personality Disorder: A Randomized Controlled Trial

Led by Fatima Jinnah Women University · Updated on 2025-09-02

60

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the impact of Mindful Self-Compassion (MSC) therapy on individuals diagnosed with Borderline Personality Disorder (BPD). This study aims to see if MSC therapy can reduce self-harm behaviors, improve emotional regulation, and enhance quality of life. The research is structured as a randomized controlled trial to provide strong evidence on the therapy's effects, which may help guide better treatment approaches for BPD. The study is conducted in two phases. The first phase involves a cross-sectional survey assessing several factors including quality of life, emotional regulation, psychological distress, self-harm behaviors, social support, and mindfulness. In the second phase, participants who have BPD with psychological distress, low social support, and low quality of life are randomly assigned to either an intervention group receiving MSC therapy or a waitlist control group. The MSC therapy is delivered in person and individually over eight weeks, covering topics like mindfulness, self-kindness, and resilience building. After the study concludes, the control group will also be offered the therapy. Participants will be assessed before and after the therapy period to compare changes in the measured outcomes. Evaluations include questionnaires on quality of life using the World Health Organization Quality of Life Scale Urdu Version at three months. The study involves regular monitoring of emotional and behavioral changes, with a focus on self-harm and emotional regulation. Overall, the study provides a detailed look at how MSC therapy may influence well-being in people with BPD over the course of the intervention and follow-up.

CONDITIONS

Brief Title

Impact of Mindful Self-Compassion Therapy on Self Harm Behaviors, Emotional Regulation and Quality of Life Among Patients With Borderline Personality Disorder

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First time diagnosed non-hospitalized patients of Borderline Personality Disorder
  • Experiencing psychological distress, low quality of life, low social support, or emotional dysregulation
  • Aged 18 years and above, both genders
  • Able to understand Urdu and provide informed consent
Not Eligible

You will not qualify if you...

  • Currently hospitalized patients with Borderline Personality Disorder
  • Patients with other chronic diseases such as cancer, cognitive deficits, or other chronic psychological disorders
  • Patients younger than 18 years old

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 8 weeks

Participants in the intervention group receive Mindful Self Compassion Therapy, an 8-week program blending mindfulness and self-compassion to improve emotional resilience and well-being.

Weekly individual in-person therapy sessions

Outpatient Treatment

Duration - 8 weeks

Participants in the waitlist control group do not receive therapy during the study period but will receive the intervention after study completion.

Follow-up

Duration - Up to 3 months after treatment

Pre- and post-assessments are conducted to evaluate the impact of Mindful Self Compassion Therapy on self-harm behaviors, emotional regulation, and quality of life.

1 post-treatment assessment visit

Trial Site Locations

Total: 2 locations

1

Commandant Afimh

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

2

Farid Family Hospital

Rawalpindi, Punjab Province, Pakistan, 46000

Actively Recruiting

Loading map...

Research Team

A

Asma Mansoor, PhD Scholar

S

Sajida Naz, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

Similar Trials

A Feasibility Trial of Eye Movement Desensitization and Repr...

Post Traumatic Stress Symptoms

Actively Recruiting

1 location

A Health Apps for Post-Pandemic Years (HAPPY) for People Wit...

Physiological Stress

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here