Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06456931

Comparing the Efficacy of Traditional Buddhist Mindfulness Training Versus Secular Mindfulness-based Cognitive Therapy for Residual Depressive Symptoms in Patients With Depressive Disorders: a Pilot Randomized Controlled Trial

Led by Anuradha Baminiwatta · Updated on 2024-06-13

60

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

A

Anuradha Baminiwatta

Lead Sponsor

C

Curtin University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating and comparing two types of mindfulness training for patients with depressive disorders who have residual symptoms. The study aims to see if traditional Buddhist mindfulness training is not worse than secular mindfulness-based cognitive therapy (MBCT) in reducing depression symptoms and improving psychological wellbeing. It also explores how both approaches affect self-compassion, mindfulness, and spirituality, as well as their role in preventing relapse over 6 and 12 months. Factors like religiosity and self-compassion are studied to understand their influence on treatment effects. Participants are randomly assigned to one of two groups. One group receives an 8-week traditional Buddhist mindfulness program with weekly 2-hour group sessions that include meditation practices, Buddhist teachings, and optional religious rituals. The other group follows the manualized secular MBCT program with weekly 2-hour sessions involving meditation, cognitive exercises, and guided home practice. Both groups are encouraged to practice daily at home for about 40 minutes. The study is conducted at a teaching hospital and a university medical faculty. During the study, participants are assessed at baseline and after 8 weeks for depression severity (using Beck Depression Inventory-II), psychological wellbeing, mindfulness, self-compassion, and spirituality. Researchers monitor depressive relapses at 6 months and 1 year after intervention. The study uses questionnaires and interviews to collect data. Safety and feasibility are also evaluated. The total study duration includes 8 weeks of intervention plus 12 months of follow-up.

CONDITIONS

Brief Title

A Pilot Study Comparing the Efficacy of Traditional Buddhist Mindfulness Training Versus Secular Mindfulness-based Cognitive Therapy for Patients Having Residual Depressive Symptoms

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 or above
  • Identify as Buddhist
  • History of one or more episodes of moderate or severe depression
  • Currently have mild to moderate depressive symptoms with a Beck Depression Inventory-II score greater than 13
Not Eligible

You will not qualify if you...

  • Currently experiencing a severe depressive episode
  • Currently having moderate to severe suicidal thoughts
  • Recent changes in antidepressant medication
  • Unable to understand and communicate in Sinhalese language

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)

Outpatient Treatment

Duration - 8 weeks

Participants undergo an 8-week program involving weekly 2-hour mindfulness sessions combined with daily home practice. One group receives traditional Buddhist mindfulness training including meditation and Buddhist teachings, while the other group receives secular mindfulness-based cognitive therapy with guided meditations and cognitive exercises.

Weekly visits for 8 weeks

Follow-up

Duration - 12 months

Participants are monitored for depressive relapses and psychological wellbeing over 12 months after completing the mindfulness training.

Visits at 6 months and 12 months post-intervention

Trial Site Locations

Total: 1 location

1

Colombo North Teaching Hospital

Ragama, Gampaha, Sri Lanka, 11010

Actively Recruiting

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Research Team

A

Anuradha Baminiwatta, MBBS, MD

M

Miyuru Chandradasa, MBBS, MD, MRCPsych

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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