Skip to content

Effects of Multimodal Training of Combined Cognitive and/or Physical Training on Cognition and Fitness of Older Adults

Effects of Multimodal Training of Combined Cognitive and Physical and Cognitive or Physical Training Only on Cognition and Physical Fitness of Older Adults: A Cluster Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04727450
Acronym
MTCCP
Enrollment
228
Registered
2021-01-27
Start date
2021-04-01
Completion date
2023-03-31
Last updated
2021-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Decline, Cognitive Impairment, Mild

Keywords

Intervention programs, Older adults, Cognitive & Physical Training, Cluster RCT, Multimodal

Brief summary

The elderly population worldwide is expected to increase exponentially. There will be a higher percentage of older adults suffering cognitive decline in the coming decades. Cognitive impairment, being the most common health problem associated with ageing, contributes to possible loss of functional independence and disability. The purpose of this study is to determine the effectiveness of four mixed modalities of three training programs (combined cognitive and physical training \[CCPT\], cognitive or physical training only) on cognition and fitness of community-dwelling older adults in Hong Kong. The study hypotheses will be set as the integrated format of all three training will have higher cognition and fitness scores than other combinations of two training modes and all these mixed modalities will have greater positive outcomes than the active control subjects.

Detailed description

The study design is a cluster randomized controlled trial. Twenty-four elderly centers as clusters will be randomly selected and assigned to be intervention (n=20) or control groups (n=4) in two study phases. A total of 8-10 older adults (age ≥ 60) from each cluster (total subjects = 228) will be invited to be study participants. Each intervention cluster will receive either an integrated training format or one out of three combinations of two training modes. Each intervention training mode will last for 2-month of 16 sessions in total, 2 sessions per week and 60 min per session, hence, the total intervention will last for 4 months for two training modes or an integrated training format. Assessments will be conducted at pre-test, two post-training tests, and a 2-month follow-up test after completion of all training.

Interventions

BEHAVIORALCognitive training

Involves participants engaging in selected games which require thinking skills to be played in a group of 2-4 people.

BEHAVIORALphysical training

Involves learning of preselected routines of line dancing taught by a line dance instructor.

BEHAVIORALCombination of cognitive and physical training (CCPT)-BIGMAP

BIGMAP is a program engaging participants in specially designed cognitive/memory games together with physical training (Fu & Chow, 2019).

Sponsors

Jacobs University Bremen gGmbH
CollaboratorOTHER
The Hong Kong Polytechnic University
CollaboratorOTHER
Hong Kong Baptist University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

No information will be given to test administrators about intervention or control groups with the exception of project staff.

Intervention model description

Cluster RCT. Each elderly center as a cluster will be randomly assigned to be either an intervention group (IG) to receive intervention training modes (A: cognitive training, B: physical training only, C: CCPT) or a control group (CG). IGs will either receive integrated format of ABC or two training modes of AB or BC or CA.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age 60 or above 2. Both gender 3. Willingness and capability to participate in this study and training 4. Willingness and capability to give informed consent to participate in this study 5. Pass the cutting-point of referenced screening tests (cognitive and emotional) Screening tools: * MOCA score above 19 (satisfactory basic function) * Positive and Negative Syndrome Scale (PANSS) with scores \< 19 in positive scale, \< 22 in negative scale, and \< 38 in general psychopathology scale

Exclusion criteria

1. A history of systematic cardiovascular diseases, poorly controlled hypertension, stroke, Parkinson's disease 2. Early stages of Alzheimer's Disease, or the use of psychoactive drugs 3. Complicated conditions that preclude regular attendance of the training 4. Currently receiving regular physical (perform aerobic, flexibility and stretching exercises for 3 days per week, 45 minutes per session, for 1 year or longer) and cognitive exercises (such as playing mahjong, chess, bridge and reading for more than 30 minutes per session and 3 times per week, for 1 year or longer ).

Design outcomes

Primary

MeasureTime frameDescription
Cognitive Tests: for everyday memory (4th test)4th test: after 2-month follow upRivermead Behavioral Memory Test (RBMT) for everyday memory will be conducted (30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for everyday memory (3rd test)3rd test: after 4-month interventionRivermead Behavioral Memory Test (RBMT) for everyday memory will be conducted (30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for everyday memory (2nd test)2nd test: after 2-month interventionRivermead Behavioral Memory Test (RBMT) for everyday memory will be conducted (30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for everyday memory (pre-test)Pre-test (1st test): before interventionRivermead Behavioral Memory Test (RBMT) for everyday memory will be conducted (30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for attention (4th test)4th test: after 2-month follow upColor Trail Making test (CTMT) for attention will be conducted (5-8 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for attention (3rd test)3rd test: after 4-month interventionColor Trail Making test (CTMT) for attention will be conducted (5-8 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for executive function (pre-test)Pre-test (1st test): before interventionWisconsin Card Sorting Test (WCST) for the executive function will be conducted (20-30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for attention (2nd test)2nd test: after 2-month interventionColor Trail Making test (CTMT) for attention will be conducted (5-8 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for attention (pre-test)Pre-test (1st test): before interventionColor Trail Making test (CTMT) for attention will be conducted (5-8 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for executive function (4th test)4th test: after 2-month follow upWisconsin Card Sorting Test (WCST) for the executive function will be conducted (20-30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for executive function (3rd test)3rd test: after 4-month interventionWisconsin Card Sorting Test (WCST) for the executive function will be conducted (20-30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.
Cognitive Tests: for executive function (2nd test)2nd test: after 2-month interventionWisconsin Card Sorting Test (WCST) for the executive function will be conducted (20-30 min, unit on a scale) in four evaluation time frames, respectively. The evaluators at all sessions will be blind to the group membership of participants.

Secondary

MeasureTime frameDescription
Fitness Tests: Senior physical fitness test battery (3rd test)3rd test: after 4-month interventionSenior physical fitness test
Fitness Tests: Senior physical fitness test battery (2nd test)2nd test: after 2-month interventionSenior physical fitness test
Fitness Tests: BMI (pre-test)Pre-test (1st test): before interventionWeight and height will be tested and combined to report BMI in kg/m\^2 in four evaluation time frames
Fitness Tests: BMI (2nd test)2nd test: after 2-month interventionWeight and height will be tested and combined to report BMI in kg/m\^2 in four evaluation time frames
Fitness Tests: BMI (3rd test)3rd test: after 4-month interventionWeight and height will be tested and combined to report BMI in kg/m\^2 in four evaluation time frames
Fitness Tests: BMI (4th test)4th test: after 2-month follow upWeight and height will be tested and combined to report BMI in kg/m\^2 in four evaluation time frames
Fitness Tests: Senior physical fitness test battery (pre-test)Pre-test (1st test): before interventionSenior physical fitness test
Fitness Tests: Senior physical fitness test battery (4th test)4th test: after 2-month follow upSenior physical fitness test
Four square step test for dynamic balance (pre-test)Pre-test (1st test): before interventionFour square step test
Four square step test for dynamic balance (2nd test)2nd test: after 2-month interventionFour square step test
Four square step test for dynamic balance (3rd test)3rd test: after 4-month interventionFour square step test
Four square step test for dynamic balance (4th test)4th test: after 2-month follow upFour square step test

Other

MeasureTime frameDescription
Behavioral and motivation survey (pre-test)Pre-test (1st test): before interventionSurvey on motivation and subjective health status rating
Physical activity participation Survey (4th test)4th test: after 2-month follow upPhysical activity participation (TTM)
Physical activity participation Survey (3rd test)3rd test: after 4-month interventionPhysical activity participation (TTM)
Physical activity participation Survey (2nd test)2nd test: after 2-month interventionPhysical activity participation (TTM)
Physical activity participation Survey (pre-test)Pre-test (1st test): before interventionPhysical activity participation (TTM)
Depression and Loneliness Survey (4th test)4th test: after 2-month follow upThe Center for Epidemiological Studies-Depression scale (CES-D) and Loneliness
Depression and Loneliness Survey (3rd test)3rd test: after 4-month interventionThe Center for Epidemiological Studies-Depression scale (CES-D) and Loneliness
Depression and Loneliness Survey (2nd test)2nd test: after 2-month interventionThe Center for Epidemiological Studies-Depression scale (CES-D) and Loneliness
Depression and Loneliness Survey (pre-test)Pre-test (1st test): before interventionThe Center for Epidemiological Studies-Depression scale (CES-D) and Loneliness
Behavioral and Motivation Survey (4th test)4th test: after 2-month follow upSurvey on motivation and subjective health status rating
Behavioral and motivation survey (3rd test)3rd test: after 4-month interventionSurvey on motivation and subjective health status rating
Behavioral and motivation survey (2nd test)2nd test: after 2-month interventionSurvey on motivation and subjective health status rating

Countries

Hong Kong

Contacts

Primary ContactBik-Chu CHOW, PhD
bchow@hkbu.edu.hk+85234117007
Backup ContactJojo JIAO, PhD
jojojiao@hkbu.edu+85234115758

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026