NCT07759232

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

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Trial Health Score

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

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
3mo left

Started Nov 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Completed
14 days until next milestone

First Posted

Study publicly available on registry

August 12, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

November 16, 2026

Expected
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 18, 2027

21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 8, 2027

Last Updated

August 12, 2026

Status Verified

July 1, 2026

Enrollment Period

2 months

First QC Date

July 29, 2026

Last Update Submit

August 6, 2026

Conditions

Keywords

Exercise SnacksHigh-intensity Interval TrainingCognitive FunctionPhysical ActivityPrefrontal CortexNeurodevelopmental disordersintellectual disability

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 INTERVENTION

Participants maintain their usual daily activities without additional prescribed exercise. Daily physical activity will be recorded throughout the intervention period.

Arm 2(Exercise Snacks)

EXPERIMENTAL

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

Behavioral: Exercise Snacks

Arm 3(High-Intensity Interval Training )

EXPERIMENTAL

One 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.

Behavioral: High-Intensity Interval Training

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.

Arm 3(High-Intensity Interval Training )
Exercise SnacksBEHAVIORAL

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

Arm 2(Exercise Snacks)

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Conditions

Intellectual DisabilityMotor ActivityNeurodevelopmental Disorders

Interventions

High-Intensity Interval Training

Condition Hierarchy (Ancestors)

Neurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsMental DisordersBehavior

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Zhaowei Kong, PhD

    University of Macau

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yuping Zhou, master

CONTACT

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

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.

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.

Locations