NCT07546916

Brief Summary

This study examines whether a single session of exergaming-based seated Tai Chi can acutely improve working memory, executive function, and prefrontal cortical efficiency in younger and older adults, compared with seated stretching. Using a within-subject crossover design, 40 participants aged 18-30 years and 60-75 years will complete both conditions in counterbalanced order on separate days. Cognitive performance will be assessed with Flanker and n-back tasks, while prefrontal activity will be recorded with fNIRS over the dorsolateral, ventrolateral, and frontopolar prefrontal cortex. Neural efficiency will be estimated by integrating task performance with task-evoked oxygenated hemoglobin responses. The Tai Chi intervention is a 40-minute seated, exergame-guided 12-form routine preceded and followed by brief warm-up and cool-down periods. The control condition is a time-matched seated stretching programme without Tai Chi-specific movements or game feedback. Both conditions will be delivered at light-to-moderate intensity and supervised for safety and adherence. The study tests whether acute exergaming-based seated Tai Chi produces greater post-intervention improvements in cognitive performance and more efficient prefrontal activation than stretching, and whether these effects differ by age group. Findings may clarify how a feasible seated mind-body exergame influences acute cognitive and neural responses across the adult lifespan.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P50-P75 for not_applicable healthy

Timeline
10mo left

Started Jun 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 8, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2027

Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

10 months

First QC Date

April 8, 2026

Last Update Submit

April 20, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Prefrontal cortical activation during inhibitory control (Flanker task)

    Prefrontal cortical activity (oxyhemoglobin concentration, µM) will be recorded using functional near-infrared spectroscopy (fNIRS) during the Eriksen Flanker Task, which assesses inhibitory control. Regions of interest include the dorsolateral prefrontal cortex (DLPFC), ventrolateral prefrontal cortex (VLPFC), and frontopolar prefrontal cortex (FPC). Measurements will be taken before and immediately after a single session of exergaming-based seated Tai Chi and a single session of seated stretching in a crossover design. Data will be reported separately for each condition. Unit of Measure: µM (micromolar) oxyhemoglobin concentration.

    Baseline (pre-session) and immediately post-session on 2 consecutive days (Day 1 and 2).

  • Prefrontal cortical activation during working memory (n-back task)

    Prefrontal cortical activity (oxyhemoglobin concentration, µM) will be recorded using functional near-infrared spectroscopy (fNIRS) during the n-back Task, which assesses working memory. Regions of interest include the dorsolateral prefrontal cortex (DLPFC), ventrolateral prefrontal cortex (VLPFC), and frontopolar prefrontal cortex (FPC). Measurements will be taken before and immediately after a single session of exergaming-based seated Tai Chi and a single session of seated stretching in a crossover design. Data will be reported separately for each condition. Unit of Measure: µM (micromolar) oxyhemoglobin concentration.

    Baseline (pre-session) and immediately post-session on 2 consecutive days (Day 1 and Day 2)

Secondary Outcomes (4)

  • Inhibitory Control Performance on the Eriksen Flanker Task - reaction time

    Baseline (Pre-Session) and Immediately Post-Session on 2 consecutive days (Day 1 and Day 2)

  • Working Memory Performance on the n-back Task - reaction time

    Baseline (Pre-Session) and Immediately Post-Session on 2 consecutive days (Day 1 and Day 2).

  • Title: Working Memory Performance on the n-back Task - Accuracy

    Baseline (Pre-Session) and immediately post-session on 2 consecutive days (Day 1 and Day 2).

  • Inhibitory Control Performance on the Eriksen Flanker Task - Accuracy

    Baseline (Pre-Session) and immediately post-session on 2 consecutive days (Day 1 and Day 2)

Study Arms (2)

Seated stretching

ACTIVE COMPARATOR

In the seated stretching condition, participants will complete a series of structured, low-intensity exercise program that would contain comparable social interaction and enjoyment without providing any strength and balance training benefits of Tai Chi. This will match in overall duration and approximate movement amplitude to the Tai Chi sequence but without game-based feedback or Tai Chi-specific components.

Behavioral: Seated Stretching

Exergaming based sitting Tai Chi

EXPERIMENTAL

An acute exergaming-based seated Tai Chi protocol will be adapted from a newly developed 12-week training programme by our team, and will be further aligned with acute Tai Chi session parameters reported by a previous Tai Chi study, including comparable total duration, work-rest structure, and target light-to-moderate intensity. Participants will perform upper-limb and trunk movements derived from traditional Tai Chi forms, adapted for a seated posture and integrated into an interactive exergame environment that provides visual feedback and performance scoring to enhance engagement and standardize practice. Movements will be paced using on-screen cues and visual and auditory signals to control tempo across participants.

Behavioral: Exergaming based sitting Tai Chi

Interventions

An acute exergaming-based seated Tai Chi protocol will be adapted from a newly developed 12-week training programme by our team, and will be further aligned with acute Tai Chi session parameters reported by a previous Tai Chi study, including comparable total duration, work-rest structure, and target light-to-moderate intensity. Participants will perform upper-limb and trunk movements derived from traditional Tai Chi forms, adapted for a seated posture and integrated into an interactive exergame environment that provides visual feedback and performance scoring to enhance engagement and standardize practice. Movements will be paced using on-screen cues and visual and auditory signals to control tempo across participants.

Also known as: Active control
Exergaming based sitting Tai Chi

In the seated stretching condition, participants will complete a series of structured, low-intensity exercise program that would contain comparable social interaction and enjoyment without providing any strength and balance training benefits of Tai Chi. This will match in overall duration and approximate movement amplitude to the Tai Chi sequence but without game-based feedback or Tai Chi-specific components.

Also known as: Intervention
Seated stretching

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Are aged 18-30 years (young adult group) or 60-75 years (older adults)
  • Have no current regular participation (e.g., ≥1 session/week) in Tai Chi, martial arts, or other mind-body exercise (e.g., yoga or qigong) in the last 3-6 months
  • Have no self-reported or clinically documented history of mild cognitive impairment, dementia, or other neurological (e.g., stroke) or psychiatric disorders (e.g., schizophrenia) known to affect cognition
  • Score within the normal range on the Hong Kong version of Montreal Cognitive Assessment (HK-MoCA) based on established age- and education-adjusted cutoffs
  • Are medically stable, with or without controlled chronic conditions (e.g., controlled hypertension or diabetes)
  • Are able to tolerate light-to-moderate seated exercise (Chinese version of Physical Activity Readiness Questionnaire score = 0)
  • Have no significant sensory impairment (e.g., vision) not corrected by assistive devices (e.g., glasses)
  • Are not engaged in regular structured exercise involving moderate-to-vigorous intensity physical activity (e.g., brisk walking, running, or racquet sports) more than two times per week over the preceding three months

You may not qualify if:

  • Have medical conditions that may interfere with safe participation, including pacemaker implantation or prosthetic devices
  • Have serious orthopedic or cardiovascular disorders that could affect participation in exergaming training
  • Have significant motor or balance impairment that would prevent performing basic seated arm and trunk movements
  • Are currently undergoing other clinical trials or structured exercise or cognitive training programmes \>2 times/week during the preceding three months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Exergaming Research Centre, Hong Kong Metropolitan University

Ho Man Tin, Kowloon, Hong Kong

Location

Related Publications (1)

  • Wang H, Guo Y, Fan H, Chen Z, Liu S, Zhao L, Shi Y. The effects of an acute Tai Chi on emotional memory and prefrontal cortex activation: a fNIRS study. Front Behav Neurosci. 2025 Jan 22;18:1520508. doi: 10.3389/fnbeh.2024.1520508. eCollection 2024.

    PMID: 39911243BACKGROUND

MeSH Terms

Interventions

Methods

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Officials

  • Tai Wa Liu

    School of Nursing and Health Sciences, Hong Kong Metropolitan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

April 8, 2026

First Posted

April 23, 2026

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

March 31, 2027

Study Completion (Estimated)

March 31, 2027

Last Updated

April 23, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will share

Non-identifiable individual participant data is available upon reasonable request to the corresponding author after the report published.

Shared Documents
SAP
Time Frame
After the study published.

Locations