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Effects of Exercise Snacks on Physical Health and Cognitive Function in Individuals With Intellectual Disabilities

Effects of Exercise Snacks on Physical Health and Cognitive Function in Individuals With Intellectual Disabilities

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07759232
Enrollment
24
Registered
2026-08-12
Start date
2026-11-16
Completion date
2027-02-08
Last updated
2026-08-12

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

Conditions

Intellectual Disability

Keywords

Exercise Snacks, High-intensity Interval Training, Cognitive Function, Physical Activity, Prefrontal Cortex, Neurodevelopmental disorders, intellectual disability

Brief summary

Intellectual disability (ID) is a neurodevelopmental disorder accompanied by sedentary lifestyles, which worsens cognitive function and physical health. Short-duration high-frequency exercise snacks (ES) may be a feasible intervention for adults with ID. This randomized controlled crossover study aims to explore the acute effects of exercise snacks, conventional HIIT and daily routine control on cognitive function, stereotyped behaviors and prefrontal cortex activation in adults with mild to moderate ID. All participants will receive three intervention conditions with a 1-week washout period between each trial. Neurophysiological indicators including EEG and heart rate variability will be measured to reveal the underlying mechanisms.

Detailed description

Background: Adults with intellectual disability commonly maintain sedentary daily routines, resulting in progressive decline in physical fitness and cognitive performance. Traditional long-duration exercise interventions are difficult to implement for this population due to behavioral and cognitive limitations. Exercise snacks, consisting of repeated ultra-short exercise bursts, are easy to carry out and show promising benefits for cognition. Methods: A randomized controlled crossover design will be adopted. Twenty-four adults aged 18-35 years with mild to moderate ID will complete three conditions in random sequence: no-exercise control, high-intensity interval training (HIIT), and exercise snacks (ES). A 1-week washout interval separates different interventions. Intervention protocols: 1. Control: maintain habitual daily activities. 2. HIIT: one afternoon session, 10 sets of 6-second high-knee exercise with 9 seconds rest. 3. ES: morning and afternoon sessions every day; each session contains 5 sets of 6-second high-knee exercise with 9 seconds rest. Main measurements include prefrontal cortex activation via EEG, cognitive function, stereotyped behaviors, and heart rate variability. Repeated-measures statistical models will be used for data analysis.

Interventions

BEHAVIORALHigh-Intensity Interval Training

Acute high-intensity interval training protocol: 10 × 6 s high-knee exercise with 9 s rest between sets, completed in a single afternoon session.

BEHAVIORALExercise Snacks

Twice-daily short-bout exercise snacks. Each session includes 5 sets of 6-second high-knee exercise with 9 seconds rest between sets.

Sponsors

University of Macau
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 18-35 years old; 2. Clinically diagnosed mild to moderate intellectual disability; 3. Able to follow simple verbal instructions and complete exercise protocols; 4. No contraindications for moderate physical activity confirmed by medical inquiry; 5. Participants or legal guardians provide written informed consent; 6. Maintain stable daily routine and do not participate in other structured exercise programs during the trial.

Exclusion criteria

1. Severe physical disabilities, orthopedic injury or neurological disorders that restrict movement; 2. History of cardiovascular disease, uncontrolled hypertension or other exercise contraindications; 3. Current psychiatric medication that significantly affects motor or cognitive function; 4. Inability to cooperate with EEG and physiological signal collection; 5. Pregnancy; 6. Participation in other interventional studies within the past 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Changes in cognitive function assessed by cognitive test batteryBaseline and immediately after the acute interventionChanges in cognitive performance measured after each intervention condition, including attention and executive function.

Secondary

MeasureTime frameDescription
Prefrontal cortex activation measured by electroencephalography (EEG)Baseline and immediately after the acute interventionChanges in prefrontal cortical brain activity indexed by EEG power spectrum during cognitive tasks.

Countries

China

Contacts

CONTACTYuping Zhou, master
yc57146@um.edu.mo+86-18811611796
PRINCIPAL_INVESTIGATORZhaowei Kong, PhD

University of Macau

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026