Tai Chi/Qigong for Subsyndromal Depression and Cognition in Older Age Bipolar Disorder

NCT ID: NCT04450147

Last Updated: 2025-05-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

23 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-10

Study Completion Date

2021-05-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

It is expected that by 2030, the percentage of patients with bipolar disorder (BD) in Canada over 60 years of age will exceed 50%. In this population, poor cognition and persistent sub-threshold depressive symptoms are particularly common, difficult to treat, associated with increased mood episodes, and poor daily functioning. Mind-body interventions have increasingly been found to be effective in treating several psychiatric condition including BD. A few pilot studies examining mindfulness-based intervention in younger adult BD have been promising for depressive symptoms, but some pilot research suggest that patients with older age bipolar disorder (OABD) may benefit more from moving mindfulness. The investigators will conduct a 12-week randomized controlled trial to assess whether tai-chi/qigong will be associated with 1) greater reduction in depressive symptoms, and 2) greater improved cognition, in comparison to a light exercise active control condition, 12- and 24-weeks from baseline, in BD patients aged 40+.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bipolar Disorder

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Tai Chi and Qigong

50mins x 12 weeks of virtually-delivered group tai chi/qigong

Group Type EXPERIMENTAL

Tai Chi/Qigong vs. Walking/Stretching

Intervention Type BEHAVIORAL

Both interventions can be thought of as a form of movement and exercise.

Walking and Stretching

50mins x 12 weeks of virtually-delivered group walking and stretching

Group Type ACTIVE_COMPARATOR

Tai Chi/Qigong vs. Walking/Stretching

Intervention Type BEHAVIORAL

Both interventions can be thought of as a form of movement and exercise.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Tai Chi/Qigong vs. Walking/Stretching

Both interventions can be thought of as a form of movement and exercise.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* aged greater than or equal to 40 years
* history of diagnosis of bipolar I or II disorder
* access to a computer with a functioning camera, microphone, and ability to run Zoom software
* English or French speaking
* ability to give informed consent

Exclusion Criteria

* Young Mania Rating Scale score \> 5
* current clinician diagnosis of substance abuse, unless currently in complete remission
* risk of suicide as assessed by a score above 3 on item 10 of Montgomery Asberg Depression Rating Scale
* participation or plan to participate in any other concurrent psychosocial group program during course of study
* unstable psychiatric medication (less than 4-weeks since commencement)
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Lady Davis Institute

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Soham Rej MD, MSc

Geriatric Psychiatrist, Assistant Professor, Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Lady Davis Institute

Montreal, , Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

References

Explore related publications, articles, or registry entries linked to this study.

Sajatovic M, Eyler LT, Rej S, Almeida OP, Blumberg HP, Forester BP, Forlenza OV, Gildengers A, Mulsant BH, Strejilevich S, Tsai S, Vieta E, Young RC, Dols A. The Global Aging & Geriatric Experiments in Bipolar Disorder Database (GAGE-BD) project: Understanding older-age bipolar disorder by combining multiple datasets. Bipolar Disord. 2019 Nov;21(7):642-649. doi: 10.1111/bdi.12795. Epub 2019 May 30.

Reference Type BACKGROUND
PMID: 31081573 (View on PubMed)

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MP-05-2020-1825

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Qigong Relaxation Exercise
NCT07294443 COMPLETED NA
Yoga in Older Cardiac Patients
NCT06235658 RECRUITING NA