NCT07446062

Brief Summary

The goal of this clinical trial is to learn if a web-based exercise and cognitive training (physical-cognitive) program works to improve movements and brain function in adults with long-term stroke. It will also learn whether the program is safe and enjoyable. The main questions it aims to answer are: Does the program improve walking, balance, strength, and reduce fall risk? Does the program improve cognitive skills such as memory, attention, and problem-solving? Researchers will compare the online exercise-and-cognitive training program to usual care to see if the program leads to greater improvements. Participants will:

  • Be randomly assigned to either the online training group or the usual care group
  • If in the training group, complete the home-based program for 12 weeks.
  • Take part in physical and cognitive tests before and after the program

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
52

participants targeted

Target at P50-P75 for not_applicable stroke

Timeline
9mo left

Started Feb 2026

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress34%
Feb 2026Mar 2027

Study Start

First participant enrolled

February 1, 2026

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

February 18, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

March 3, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2027

Last Updated

March 3, 2026

Status Verified

February 1, 2026

Enrollment Period

9 months

First QC Date

February 18, 2026

Last Update Submit

February 25, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Executive function

    Trail Making Test (TMT) part B-A will be evaluated at baseline and 3 months.

    3 months

  • Fall risk

    Fall risk will be assessed using the Timed Up and Go (TUG) test at baseline and 3 months. The time taken to complete TUG will be recorded in Sec.

    3 months

  • Gait speed

    10-Meter Walk test (10MWT) will be used to assessed gait speed at baseline and 3 months.

    3 months.

Secondary Outcomes (7)

  • Global cognitive function

    3 months

  • Attention

    3 months

  • Motor function

    3 months

  • Balance

    3 months

  • Muscle strength

    3 months

  • +2 more secondary outcomes

Study Arms (2)

Web-Based Physical-Cognitive Telerehabilitation Exergaming

EXPERIMENTAL

Physical-cognitive exergame via web-based platform at home setting for 60 min/session, 3 sessions/week for 12 weeks.

Behavioral: Web-Based Physical-Cognitive Telerehabilitation Exergaming

Control

NO INTERVENTION

Interventions

Perform a physical-cognitive exergame via ExerbrainCMU web-based platform at home setting for 60 min/session, 3 sessions/week for 12 weeks.

Web-Based Physical-Cognitive Telerehabilitation Exergaming

Eligibility Criteria

Age20 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • diagnosed with ischemic or hemorrhagic stroke at least 6 months before enrollment
  • aged between 20 and 80 years
  • able to walk at least 10 meters with or without assistive devices
  • able to perform sit-to-stand safely with or without assistive devices
  • can see the screen of a tablet or notebook computer at a distance of at least 60 cm
  • have a stable medical condition and can follow study instructions
  • frequent users of a mobile phone, tablet, or notebook computers

You may not qualify if:

  • have medical conditions or complications that would be unsafe to exercise
  • have neglect, impaired communication, or uncorrected visual problems \[30\], or - have severe spasticity of the upper or lower extremities (Modified Ashworth Scale ≥ 3)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

StrokeMotor Activity

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesBehavior

Study Officials

  • Puntarik Keawtep

    Chiang Mai Uiversity

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Puntarik Keawtep, Ph.D., Primary investigator

CONTACT

Somporn Sungkarat, PhD, Associate Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: A two-arm, assessor blind, and randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

February 18, 2026

First Posted

March 3, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

March 1, 2027

Last Updated

March 3, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual Participant Data (IPD) will not be shared because the informed consent obtained from participants did not include permission for public data sharing. Additionally, due to the sensitive nature of the clinical data and the potential risk of participant re-identification, data sharing is not planned.