Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07341438

Physical Activity in the Management of Personality Disorders: Protocol for a Three-Arm Randomized Feasibility Trial (The PANDA Trial)

Led by Julie Midtgaard · Updated on 2026-02-03

60

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

Sponsors

J

Julie Midtgaard

Lead Sponsor

D

Danish Council for Independent Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the safety, feasibility, and acceptability of two types of physical activity—an 8-week pedometer-based walking program and supervised karate training—combined with usual treatment for adults diagnosed with borderline or avoidant personality disorders. The study aims to explore whether these activities are manageable and safe while observing possible effects on physical health, fitness, emotions, personality symptoms, body image, and daily activity. This trial will help determine if a larger study can be done in the future to assess benefits for people with these personality disorders. Participants are randomly assigned to one of three groups: usual treatment only, usual treatment plus the walking program, or usual treatment plus supervised karate training. The walking program involves tailored goals, daily step recording with a pedometer, and regular check-ins over 8 weeks. The karate program includes twice-weekly group sessions led by experienced instructors, featuring meditation, basic karate techniques, partnered exercises, and stretching. After the 12-week follow-up, those in the control or walking groups may choose to join the karate program. Participants attend assessments at baseline, 8 weeks, and 12 weeks, including physical tests like body composition and cardiorespiratory fitness, and self-report questionnaires. The 12-week follow-up questionnaires can be completed online at home. Safety is monitored through bi-weekly questionnaires for adverse events during the intervention period and medical record reviews through follow-up. Interviews with some participants will explore their experiences and views on the activities. The total study participation lasts about 12 weeks, with some continuing karate training afterward if desired.

CONDITIONS

Brief Title

Physical Activity in the Management of Personality Disorders

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosed with borderline personality disorder (BPD) or avoidant personality disorder (AVPD) confirmed in medical records
  • Currently receiving treatment at one of two specialized psychotherapeutic outpatient clinics in the Capital Region of Denmark
  • Proficient in Danish
Not Eligible

You will not qualify if you...

  • Diagnosis of antisocial personality disorder (F60.2)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants undergo one of three interventions: supervised karate training twice weekly for 8 weeks, an 8-week pedometer-based walking program with regular check-ins, or treatment as usual within psychiatric services.

2 in-person visits (baseline and 8 weeks), plus additional phone or online check-ins for walking group

Follow-up

Duration - 4 weeks

Participants complete final assessments through online questionnaires to evaluate outcomes after the intervention period.

1 online visit at 12 weeks

Trial Site Locations

Total: 2 locations

1

Mental Health Center Stolpegård, Copenhagen University Hospital -Mental Health Services CPH, Copenhagen Denmark

Gentofte Municipality, Capital Region, Denmark, 2820

Actively Recruiting

2

Mental Health Centre Glostrup, Copenhagen University Hospital - Amager and Hvidovre, Denmark

Glostrup Municipality, Capital Region, Denmark, 2620

Actively Recruiting

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Research Team

J

Justina Petersen, PhD student

I

Ida Lundager Kraaer

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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