Effects of Exercise Snacks on Physical Health and Cognitive Function in Individuals With Intellectual Disabilities
1 other identifier
interventional
24
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 29, 2026
CompletedFirst Posted
Study publicly available on registry
August 12, 2026
CompletedStudy Start
First participant enrolled
November 16, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 18, 2027
Study Completion
Last participant's last visit for all outcomes
February 8, 2027
August 12, 2026
July 1, 2026
2 months
July 29, 2026
August 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Changes in cognitive function assessed by cognitive test battery
Changes in cognitive performance measured after each intervention condition, including attention and executive function.
Baseline and immediately after the acute intervention
Secondary Outcomes (1)
Prefrontal cortex activation measured by electroencephalography (EEG)
Baseline and immediately after the acute intervention
Study Arms (3)
Arm 1
NO INTERVENTIONParticipants maintain their usual daily activities without additional prescribed exercise. Daily physical activity will be recorded throughout the intervention period.
Arm 2(Exercise Snacks)
EXPERIMENTALTwice-daily short-bout exercise snacks. Each session includes 5 sets of 6-second high-knee exercise with 9 seconds rest between sets.
Arm 3(High-Intensity Interval Training )
EXPERIMENTALOne intervention session scheduled in the afternoon. The protocol consists of 10 sets of 6-second high-knee exercise, separated by 9 seconds of rest between sets.
Interventions
Acute high-intensity interval training protocol: 10 × 6 s high-knee exercise with 9 s rest between sets, completed in a single afternoon session.
Twice-daily short-bout exercise snacks. Each session includes 5 sets of 6-second high-knee exercise with 9 seconds rest between sets.
Eligibility Criteria
You may qualify if:
- Aged 18-35 years old;
- Clinically diagnosed mild to moderate intellectual disability;
- Able to follow simple verbal instructions and complete exercise protocols;
- No contraindications for moderate physical activity confirmed by medical inquiry;
- Participants or legal guardians provide written informed consent;
- Maintain stable daily routine and do not participate in other structured exercise programs during the trial.
You may not qualify if:
- Severe physical disabilities, orthopedic injury or neurological disorders that restrict movement;
- History of cardiovascular disease, uncontrolled hypertension or other exercise contraindications;
- Current psychiatric medication that significantly affects motor or cognitive function;
- Inability to cooperate with EEG and physiological signal collection;
- Pregnancy;
- Participation in other interventional studies within the past 3 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hangzhou First Social Welfare Institute
Hangzhou, Zhejiang, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Zhaowei Kong, PhD
University of Macau
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 29, 2026
First Posted
August 12, 2026
Study Start (Estimated)
November 16, 2026
Primary Completion (Estimated)
January 18, 2027
Study Completion (Estimated)
February 8, 2027
Last Updated
August 12, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, ANALYTIC CODE
- Time Frame
- Data and supporting materials will be available starting 6 months following the publication of primary study outcomes, and remain accessible for up to 5 years thereafter.
- Access Criteria
- Qualified researchers who submit a methodologically sound research proposal. Requests need to be sent to the corresponding investigator and a data use agreement must be signed.
De-identified individual participant data will be available upon reasonable request to the corresponding investigator after study completion and main publication. Data sharing will be subject to a formal data use agreement.