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NCT Number: NCT07759232

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

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.

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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:

  • Control: maintain habitual daily activities.
  • HIIT: one afternoon session, 10 sets of 6-second high-knee exercise with 9 seconds rest.
  • 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

High-intensity interval training

Behavioral

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

Exercise Snacks

Behavioral

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

Primary outcomes

  1. Changes in cognitive function assessed by cognitive test battery

    Time frame: Baseline and immediately after the acute intervention

    Changes in cognitive performance measured after each intervention condition, including attention and executive function.

Secondary outcomes

  1. Prefrontal cortex activation measured by electroencephalography (EEG)

    Time frame: Baseline and immediately after the acute intervention

    Changes in prefrontal cortical brain activity indexed by EEG power spectrum during cognitive tasks.

Study contacts

Contact information is provided by the study sponsor or research team.

Yuping Zhou, master

CONTACT

[email protected]

+86-18811611796

Sponsors and collaborators

Lead sponsor

University of Macau

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 12, 2026
Registry last updated
Aug 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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