NCT07327541

Brief Summary

This study aims to evaluate the cognitive function, physical function, and pain levels of community-dwelling older adults to determine the impact of cognitive ability on physical function and pain. It also seeks to establish foundational data for strategies to prevent dementia and sarcopenia. Therefore, the purpose of this study is to measure the cognitive function (overall cognition, executive function, memory, attention, etc.), physical function (muscle mass, muscle strength, gait and balance ability), and pain of community-dwelling older adults, and to analyze the correlations between these factors.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
130

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

December 1, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 8, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

January 12, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 12, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 13, 2026

Completed
Last Updated

April 15, 2026

Status Verified

November 1, 2025

Enrollment Period

2 months

First QC Date

December 1, 2025

Last Update Submit

April 14, 2026

Conditions

Outcome Measures

Primary Outcomes (5)

  • Overall cognitive function: MoCA-K

    Cognitive function will be assessed using the MoCA-K.

    From enrollment to the end of evaluation within 1weeks

  • Skeletal Muscle Mass Index

    The skeletal muscle mass index is the sum of limb muscle mass divided by the square of height (kg/m²).

    From enrollment to the end of evaluation within 1weeks

  • Grip strength

    Grip strength will be measured using a dynamometer. The subject will sit in a chair with arms extended, elbows bent at 90 degrees, forearms at a natural angle, and wrists in a dorsal flexion position between 0 and 30 degrees. The subject will grip the dynamometer for 3 seconds, and the average value (kg) will be recorded after 3 attempts.

    From enrollment to the end of evaluation within 1weeks.

  • Lower Limb Strength

    5 Sit-to-Stand (5xSST) measures the time (seconds) it takes for the subject to transition from a seated position to a standing position and back to a seated position five times. A shorter time indicates better muscle strength. The subject is instructed to cross their arms over their chest, avoid leaning their back or legs against the chair, and perform the sit-to-stand motion five times as quickly as possible.

    From enrollment to the end of evaluation within 1weeks.

  • Level of musculoskeletal pain

    For participants with musculoskeletal pain, the level of pain will be assessed using the Numeric Pain Rating Scale (NPRS), where 10 indicates the most severe pain and 0 indicates no pain.

    From enrollment to the end of evaluation within 1weeks.

Secondary Outcomes (7)

  • The Word Memory Test

    From enrollment to the end of evaluation within 1weeks.

  • Executive function and attention

    From enrollment to the end of evaluation within 1weeks.

  • Executive function

    From enrollment to the end of evaluation within 1weeks.

  • Subjective Cognitive Decline

    From enrollment to the end of evaluation within 1weeks.

  • Static Balance in Three Positions

    From enrollment to the end of evaluation within 1weeks.

  • +2 more secondary outcomes

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants in this study will consist of community-dwelling adults aged 65 years or older who use local senior welfare centers and voluntarily agree to participate in the research.

You may qualify if:

  • Community-dwelling adults aged 65 years or older who are able to walk independently

You may not qualify if:

  • Individuals with severe cognitive impairment that makes test participation difficult (e.g., diagnosed dementia)
  • Individuals with acute neurological injury within the past 6 months (e.g., stroke)
  • Individuals for whom gait testing is not feasible for safety reasons

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sahmyook University

Seoul, Seoul, 01795, South Korea

Location

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Researcher, PhD

Study Record Dates

First Submitted

December 1, 2025

First Posted

January 8, 2026

Study Start

January 12, 2026

Primary Completion

March 12, 2026

Study Completion

April 13, 2026

Last Updated

April 15, 2026

Record last verified: 2025-11

Locations