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NCT Number: NCT07655531

Yogic Breathing Exercise and Meditation for People With Spinal Cord Disorders

The goal of the study is to understand how well yogic breathing exercise and meditation improves breathing, fatigue, emotional well-being and quality of life in people with spinal cord disorders.

Aim 1. Evaluate the efficacy of an 8-week, virtual, coach-guided yogic breathing and meditation (YBM) program on QoL and mental health in people with spinal cord disorders.

This study will include completing several questionnaires 3 times, 8 weeks of participating in 2 sessions per week of yogic breathing exercise and meditation via Zoom and being interviewed once at the completion of the 8-week program.

Recruiting

Interested in participating?

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Key information

Age range

18 year–89 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

General Information You are being asked to take part in a research study. This research study is voluntary, meaning you do not have to take part in it. The procedures, risks, and benefits are fully described further in the consent form.

Purpose The purpose of the study is to understand how well yogic breathing exercise and meditation improves breathing, fatigue, and emotional well-being in people with spinal cord injury (SCI).

Duration & Visits You will complete several questionnaires (3 different times) that will take 30 minutes to complete each time, participate in 12-30-minute yogic breathing exercise and meditation sessions (over 8 weeks), complete a 25-minute interview and that you will be in the study for 2 months.

Overview of Procedures This study will include completing several questionnaires multiple times, 8 weeks of participating in 2 sessions per week of yogic breathing exercise and meditation via Zoom and being interviewed once.

Risks The most common risks include some tiredness and frustration while learning the yogic breathing exercise and meditation techniques. Loss of confidentiality is also a risk.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • spinal cord disorders
  • community-dwelling adults aged ≥ 18 years
  • able to follow simple, three-step verbal instructions (e.g., close your eyes, open your mouth, close your mouth)
  • access to the internet and an electronic device with videoconferencing capability
  • able to set up virtual sessions with/without caregiver assistance
  • sufficient English language proficiency to provide consent for study participation and complete self-report questionnaires

Exclusion criteria

  • suicidal intent requiring emergency care
  • bedridden with continuous use of noninvasive ventilation
  • participating in weekly pulmonary PT, psychological therapy, or a clinical trial that could affect proposed study outcomes.

Treatment and study plan

yogic breathing and meditation

Behavioral

yogic breathing exercise and meditation exercise

Primary outcomes

  1. Depressive symptoms as assessed by the PHQ-9

    Time frame: change from baseline in depressive symptoms at 8 and 16 weeks

    The Patient Health Questionnaire-9 (PHQ-9) consists of nine questions inquiring about symptoms experienced over the past two weeks, ranging from low energy and sleep issues to feelings of hopelessness and self-harm. Each question is scored from 0 to 3, with a maximum total score of 27. Higher scores indicate more severe depressive symptomology.

  2. Patient health questionnaire (PHQ-9)

    Time frame: baseline, post-program (8th week), and 16th week

    The Patient Health Questionnaire-9 (PHQ-9) consists of nine questions inquiring about symptoms experienced over the past two weeks, ranging from low energy and sleep issues to feelings of hopelessness and self-harm. Each question is scored from 0 to 3, with a maximum total score of 27. Higher scores indicate more severe depressive symptomology.

Study contacts

Contact information is provided by the study sponsor or research team.

Adrian Smith, BS

CONTACT

[email protected]

12059348931

Hon Yuen, PhD

CONTACT

[email protected]

12059346301

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
Jun 18, 2026
Registry last updated
Jul 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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