ClinicalTrials.gg
Status unknownNCT05764382Updated Mar 10, 2023

Remote Tai Ji for Low Back Pain

An interventional study of T'ai Chi and Qigong Rehabilitation and Usual care in Low Back Pain, sponsored by New York Presbyterian Hospital. Status unknown at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-03-10.

Sponsored by New York Presbyterian Hospital · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2023), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The purpose of the study is to examine the implementation strategy, in terms of feasibility and the possible benefits, of a free online Zoom t'ai chi and qigong gentle movement and meditation program to reduce back pain and to improve sleep and quality of life among those with chronic back pain. The primary objective of this study is to examine whether a safe and moderate online t'ai chi and qigong exercise program, offered without cost to individuals with chronic back pain, improves pain levels, sleep, and quality of life; The secondary objective is to explore whether improvements in pain levels are different among smokers and those with unhealthy BMI than among others.

02

Conditions studied

  • Low Back Pain

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Keywords

  • Tai Chi
  • Qigong
03

In context

Low Back Pain

2,922 studies on the registry are indexed under Low Back Pain; 580 are open to participants now.

This study's planned enrollment of 300 is above the median of 60 across 2,364 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

New York Presbyterian Hospital is the lead sponsor of 20 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18 years and older
  • Have experienced low back pain for the last 6 weeks or longer
  • Understands written and spoken English
  • Be willing to complete the initial survey and 3 additional ones emailed baseline and January 2023
  • Be willing and able to provide consent to participate in the survey

Exclusion criteria

Exclusion Criteria:

  • pregnany
  • previously has taken t'ai chi classes
  • spine surgery within the last 6 months
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    T'ai Chi and Qigong Rehabilitation

    Behavioral: T'ai Chi and Qigong Rehabilitation

  • Active comparator
    Usual care

    Other: Usual care

Interventions

  • BehavioralT'ai Chi and Qigong Rehabilitation

    T'ai chi/Qigong is a multidimensional (mind, body, and spirit integrative) and multimodal (strength, flexibility, balance, posture, and light to moderate aerobic) form of exercise that is safe for persons of all ages and physical abilities. The 12-week, twice-per-week t'ai chi and qigong gentle movement and meditation program proposed to be studied is adapted from the WaQi program, a curriculum developed by Master Yang Yang, PhD. Master Yang developed this course based on his own healing journey from severe back pain following a bike accident in 2014.

  • OtherUsual care

    Usual care as per primary care physican, physical therapist.

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What researchers measure

Primary outcomes

  1. Change in the Oswestry Disability Index 3 months after intervention

    0 to 100 scale

    Time frame: baseline, 3 months

Secondary outcomes

  1. Change in visual analogue scale (VAS) for low back pain

    0-100 scale

    Time frame: baseline, 3 months

  2. Change in VAS leg pain

    0 to 100 scale

    Time frame: baseline, 3 months

  3. The "SF-36," Short Form Health Survey questionnaire

    Time frame: baseline, 3 months

  4. 9-Item Pittsburgh Sleep Quality Index

    Time frame: baseline, 3 months

07

Study locations

1 of 1 sites recruiting
  • New York Presbytarian Hospital
    New York, New York 10021, United States
    Recruiting
    • Pravesh S Gadjradj, MD · Contactpsg4001@med.cornell.edu · 212-821-0850
    • Brendan Mendary, BS · Contactbrm4011@med.cornell.edu · (212) 821-0850
    • Roger Hartl, Prof.dr. · Principal investigator
    • Sertac Kernaz, MD · Sub investigator
    • Rachel Yerden, BSc · Sub investigator
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 10, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05764382
Lead sponsor
New York Presbyterian Hospital
Collaborators
Center for Taiji and Qigong Studies & Wa-Qi.com
Responsible party
Pravesh Gadjradj (Physician, Epidemiologist, New York Presbyterian Hospital) — Principal investigator
First posted
Mar 10, 2023
Start date
Jan 1, 2023
Primary completion
Jun 1, 2023 (estimated)
Completion
Jun 1, 2023 (estimated)
Last update
Mar 10, 2023

Study contacts

Pravesh S Gadjradj, MD, MSc
Contact
p.gadjradj@erasmusmc.nl
+1‭(201) 263-1212‬
Kenneth Kapp
Contact
kenneth_knapp@nymc.edu
Yang Yang, PhD
study director · Director Center for Taiji and Qigong Studies & Wa-Qi.com https://www.wa-qi.com

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2023. You cannot join it, but the record below documents what was studied.

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