NCT07250932

Brief Summary

This study investigates the effects of somatosensory cognitive games interventions on older adults' cognitive and physical functions. The investigators plan to recruit up to 100 participants and randomly assign them to a control group or an experimental group. The experimental group will participate in somatosensory cognitive games for 12 weeks, while the control group will receive routine care. Data will be collected via questionnaires to examine whether somatosensory cognitive games can delay declines in cognitive and physical functions in older adults.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
19mo left

Started Nov 2025

Typical duration for not_applicable

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 Progress25%
Nov 2025Dec 2027

Study Start

First participant enrolled

November 1, 2025

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

November 13, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

November 26, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

November 26, 2025

Status Verified

September 1, 2025

Enrollment Period

1.1 years

First QC Date

November 13, 2025

Last Update Submit

November 18, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Montreal Cognitive Assessment (MoCA)

    MoCA is one of the key cognitive function outcomes that investigators expect to improve after somatosensory cognitive games. MoCA assesses six cognitive dimensions, with a total score of 30. A score of 26 or higher is considered normal. MoCA score of ≤24 may indicate a risk of mild cognitive impairment (MCI), while a MoCA score of ≤20 may indicate a risk of dementia.

    3 month follow-up

  • Color Trails Test (CTT)

    CTT is one of the key cognitive function outcomes that investigators expect to improve after somatosensory cognitive games. CTT is widely used to assess executive function and processing speed. The first part (CTT-1) evaluates visual-motor skills and attention, while the second part of the CTT (CTT-2) assesses sequencing and cognitive flexibility. Scoring is based on the time required to complete the test, with cutoff times of 240 seconds for CTT-1 and 330 seconds for CTT-2. Shorter completion times indicate better executive function and processing speed.

    3 month follow-up

Secondary Outcomes (2)

  • Short Physical Performance Battery (SPPB)

    3 month follow-up

  • Timed Up and Go Test (TUG)

    3 month follow-up

Study Arms (2)

Somatosensory Cognitive Game Intervention on Cognitive and Physical

EXPERIMENTAL
Other: somatosensory cognitive game

Routine care

NO INTERVENTION

no Intervention on Cognitive and Physical

Interventions

The experimental group will participate in somatosensory cognitive games for 12 weeks, twice a week, about 30 minutes per session.

Somatosensory Cognitive Game Intervention on Cognitive and Physical

Eligibility Criteria

Age65 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Elderly individuals aged 65 and above.
  • Able to communicate in Chinese (Mandarin or Taiwanese).
  • Voluntarily participate in this study and sign a written consent form.

You may not qualify if:

  • Individuals with severe visual impairments or physical mobility disabilities that prevent them from participating in the game activities designed in this study.
  • Individuals diagnosed with severe dementia who are unable to understand or participate in the research process.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 13, 2025

First Posted

November 26, 2025

Study Start

November 1, 2025

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2027

Last Updated

November 26, 2025

Record last verified: 2025-09