ClinicalTrials.gg
Active, not recruitingNCT07890974Updated Oct 23, 2026

Tai Chi Training for Persons With Multiple Sclerosis.

An interventional study of Tai Chi training in Multiple Sclerosis (MS) - Relapsing-remitting, sponsored by Karolinska Institutet. Active, not recruiting at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-23.

Sponsored by Karolinska Institutet · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 7 months after the study started (first participant enrolled Mar 2025, registered Oct 2026).
Updated Oct 23, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Tai Chi combines strength and neuromuscular training with diaphragmatic breathing, attention, imagery and relaxation. After an initial learning period, participants can practise independently, potentially supporting self-efficacy and sustained self-management. Studies in chronic disease report benefits for physical function and psychological wellbeing.

We will evaluate a 12-week Tai Chi rehabilitation programme in a clincial trial. The Multiple Sclerosis Impact Scale (MSIS-29) is the primary clinical outcome, reflecting the physical and psychological consequences of multiple sclerosis (MS). Assessments take place before training and at 12 weeks (the primary endpoint).

The study will address whether Tai Chi improves physical and mental health; reduces fatigue, anxiety, depression and pain; improves lower-limb strength, gait and balance; and improves quality of life and self-efficacy.

Read the detailed description

The randomized controlled trial compares 12 weeks of Tai Chi. The intervention comprises two 75-minute sessions each week. Clinical outcomes are measured before and after training to examine the maintenance of benefits and self-management behaviours.

Inclusion criteria are age over 18 years, definite MS diagnosis, ability to walk more than 100 m, no relapse or pharmacological treatment adjustment in the preceding eight weeks, no Tai Chi practice in the preceding six months, and ability to understand and communicate in Swedish or English. Exclusion criteria are dementia, alcoholism and serious medical comorbidity preventing participation.

Participants are recruited through MS and rehabilitation clinics in Region Stockholm, Neuro Sweden and social media advertisements. Screening confirms eligibility and provides a baseline assessment. Oral and written information is given and informed consent obtained before enrollment. Baseline data include age, sex, civil and employment status, and disease characteristics, including MS severity. Participants may withdraw without consequences for their care.

Tai Chi programme Training comprises three components: warm-up exercises to improve mobility and flexibility, reduce tension and introduce relaxed breathing; simple Tai Chi movements and a short sequence to develop coordinated, gentle weight shifts; and Standing like a Tree Qigong to develop upright posture, relaxation and breathing awareness. The programme teaches foundational skills and supports regular practice that can be integrated into daily living.

Participants are encouraged to maintain their usual activities but avoid starting additional exercise programmes during the intervention. Home Tai Chi practice is encouraged and recorded. Four make-up classes per month are available, and participants receive an instructional video to support continued practice after the supervised programme.

Clinical outcome measures MSIS-29 assesses the physical and psychological impact of MS [15]. Secondary outcomes are fatigue (FSMC), anxiety and depression (HADS), pain (BPI-SF), and lower-limb strength (30-second chair-stand). Gait is assessed with the 10-metre walk test and 6MWT, and balance with the Mini-BESTest. Quality of life is assessed with the Brunnsviken Brief Quality of Life Scale (BBQ), and self-efficacy with the Self-Efficacy for Managing Chronic Disease scale (SEMCD) [16-24]. Self-efficacy is of particular interest because confidence in managing symptoms may support continued use of rehabilitation skills.

02

Conditions studied

  • Multiple Sclerosis (MS) - Relapsing-remitting

Keywords

  • multiple sclerosis
  • rehabilitation
  • physical health
  • mental health
03

In context

Multiple Sclerosis, Relapsing-Remitting

615 studies on the registry are indexed under Multiple Sclerosis, Relapsing-Remitting; 80 are open to participants now.

This study's planned enrollment of 35 is below the median of 72 across 437 interventional studies indexed under Multiple Sclerosis, Relapsing-Remitting.

Browse Multiple Sclerosis, Relapsing-Remitting studies →

Lead sponsor

Karolinska Institutet is the lead sponsor of 1,145 studies on the registry; 274 are open to participants now.

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

04

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

Inclusion criteria are age over 18 years, definite MS diagnosis, ability to walk more than 100 m, no relapse or pharmacological treatment adjustment in the preceding eight weeks, no Tai Chi practice in the preceding six months, and ability to understand and communicate in Swedish or English. -

Exclusion criteria

Exclusion Criteria:

Exclusion criteria are dementia, alcoholism and serious medical comorbidity preventing participation.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (estimated)

Study arms

  • Other
    Tai Chi training

    Other: Tai Chi training

Interventions

  • OtherTai Chi training

    Training comprises three components: warm-up exercises to improve mobility and flexibility, reduce tension and introduce relaxed breathing; simple Tai Chi movements and a short sequence to develop coordinated, gentle weight shifts; and Standing like a Tree Qigong to develop upright posture, relaxation and breathing awareness. The programme teaches foundational skills and supports regular practice that can be integrated into daily living.

06

What researchers measure

Primary outcomes

  1. MSIS-29

    MSIS-29 assesses the physical and psychological impact of MS

    Time frame: From enrollment to the end of treatment at 12 weeks

07

Study locations

1 site
  • Karolinska Institutet
    Stockholm, Sweden
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Mar 2025 (actual). Primary completion is estimated for Dec 2027, 33 months after the start.

Of 72 non-industry interventional studies with no phase under Multiple Sclerosis, Relapsing-Remitting, half reached primary completion within 38 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 48. This study's planned 33 months is below that.

Counting every sponsor, half of 74 studies reached it within 38 months; a quarter within 16 and three quarters within 48.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 18, 2026
First posted
Oct 23, 2026
StartActual
Mar 1, 2025
Primary completionEst.
Dec 2027
CompletionEst.
Mar 2028
Last update
Oct 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 23, 2026
Show all 1 update
  1. Oct 23, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07890974
Responsible party
Manuel Zeitelhofer (PhD, Associate Professor, Karolinska Institutet) — Principal investigator
First posted
Oct 23, 2026
Start date
Mar 1, 2025
Primary completion
Dec 2027 (estimated)
Completion
Mar 2028 (estimated)
Last update
Oct 23, 2026

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 active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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