Validation of Population Characteristics and Dosage Prescriptions for Cognitive Function Intervention Benefits of Different Doses of Tai Chi in Elderly Patients With Mild Cognitive Impairment: A Real-World Cross-Sectional Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60+
SponsorLidian Chen

About this trial

This is a companion real-world external validation study of two pre-registered parent randomized controlled trials (RCTs, protocol IDs: FujianUTCM-1 and FujianUTCM-2). We aim to validate the generalizability and clinical applicability of a pre-developed machine learning prediction model (for Tai Chi intervention cognitive benefit population characteristics and individualized dose prescription) in a real-world community-dwelling population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1. Presence of mild cognitive impairment, not demented; 2. Age ≥ 60 years old; 3.Regular practice of standardized 24-form simplified Tai Chi for at least 6 months (consistent with the form used in the parent randomized controlled trials [RCTs]) ; 4.Informed consent and voluntary participation.

Disqualifiers

Geriatric Depression Scale score ≥ 9 points

Cognitive impairment caused by other reasons, taking drugs, poisoning, etc;

Suffer from severe musculoskeletal system diseases and other contraindications to exercise and are not suitable for Tai Chi training, such as those who suffer from stroke, Parkinson's disease, and have a history of lower limb arthritis, hip and knee joint replacement, etc;

Patients with severe heart, liver, kidney failure, malignant tumors, and other major diseases;

Trial population

This cross-sectional real-world external validation study will enroll 150 community-dwelling older adults aged 60 years and above, who are diagnosed with Mild Cognitive Impairment (MCI) and have regular practice of standardized 24-form simplified Tai Chi for at least 6 months (consistent with the form used in the parent RCTs). Eligible participants will be recruited from communities in Fuzhou, China, to validate the generalizability and clinical applicability of a pre-developed machine learning prediction model for Tai Chi cognitive benefit population identification.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • 24-form Simplified Tai Chi (Observational Behavioral Exposure)

    Behavioral

    This is the core observational exposure factor of this cross-sectional real-world external validation study, NOT an intervention actively assigned, implemented or manipulated by the investigator. This study only observes and records the existing long-term regular Tai Chi practice behavior (including dose, frequency and duration) of enrolled older adults with Mild Cognitive Impairment (MCI) during a single time-point cross-sectional survey, for the sole purpose of externally validating the generalizability of a pre-developed machine learning prediction model for Tai Chi cognitive benefit population identification and individualized dose prescription. No active behavioral intervention will be administered to any participant in this study.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Cross-Sectional External Validation Cohort1 intervention

Trial outcomes

Primary outcomes

1

Montreal Cognitive Assessment

Global cognition

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)

Secondary outcomes

1

Wechsler Memory Scale

Memory function

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
2

Digital Symbol test

Attention

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
3

Trial Making Test part B

Executive function

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
4

Stroop color word test

Processing speed

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)

Other outcomes

1

Blood glucose metabolism index

fasting blood glucose

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
2

Blood lipid metabolism index

total cholesterol (TC), total triglyceride (TG), low density lipoprotein (LDL), high density lipoprotein (HDL)

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
3

Resting-State Functional Magnetic Resonance Imaging: Default Mode Network Functional Connectivity Structural Magnetic Resonance Imaging: Hippocampal Volume

Resting-State Functional Magnetic Resonance Imaging (rs-fMRI) Measurement of Default Mode Network Functional Connectivity Strength Resting-state fMRI (rs-fMRI) data will be acquired using a 3.0T scanner to evaluate default mode network (DMN) functional connectivity strength, a key correlate of cognitive function. All scanning parameters, preprocessing and analysis methods are identical to our parent randomized controlled trials (FujianUTCM-1/2). Data processing uses SPM12 and CONN toolbox. 3.0T Three-Dimensional T1-Weighted Structural MRI (sMRI) Measurement of Bilateral Hippocampal Total Volume 3D T1-weighted structural MRI (sMRI) data will be acquired using a 3.0T scanner to quantify bilateral hippocampal total volume. All scanning parameters, preprocessing and volumetric analysis methods are consistent with our parent randomized controlled trials (FujianUTCM-1/2). Automated segmentation uses FreeSurfer 7.4.1 with manual visual correction.

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)
4

Core Peripheral Blood Biomarkers for Mild Cognitive Impairment (MCI)

Amyloid-beta(Aβ)、phosphorylated tau(p-tau)、Neurofilament light chain(NfL)、Glial fibrillary acidic protein(GFAP)

Time frame
Single cross-sectional assessment at the time of study enrollment (baseline visit)

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Lidian Chen

Lead sponsor

Fujian University of Traditional Chinese Medicine

Sponsor institution

Peking University Third Hospital

Collaborator

This trial is not recruiting at the moment. You can still explore other options: