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Virtual reality study tests if social gaming makes exercise more fun

NCT ID NCT07050654

Knowledge-focused Sponsor: Istituto di Sistemi e Tecnologie Industriali Intelligenti per il Manifatturiero Avanzato Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether doing virtual reality exercises with other people (multi-player) is more motivating than doing them alone. It included 86 participants: healthy teens, children with motor disorders, and older adults with conditions like stroke or COPD. Researchers measured motivation, enjoyment, and usability after single and multi-player sessions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

86 people

The number who actually took part.

Started

Sep 2025

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

12 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * For IRCCS E. Medea: patients 12 years and older with neuromotor pathologies; * For Villa Beretta: adults with neurological pathologies; * For INRCA Casatenovo: patients with chronic respiratory diseases, clinical stability for at least 4 weeks; * Healthy volunteers: healthy students aged 14-18 years. Exclusion Criteria: * Absence of appropriate cognitive abilities to interact with virtual reality software; * Presence of severe sensory deficits (visual acuity, auditory perception) such as to interfere with the administration of the proposed activities; * Poor trunk control or physical limitations (excessive spasticity or joint limitations) that impair the safe performance of the pedaling activity. Presence of epilepsy or treatment with antiepileptic drugs, where the physician highlights contraindications; * Participation in other standardized rehabilitation protocols involving lower limbs and walking. Specifically, for INRCA Casatenovo: * clinical instability (pH \<7.35, hemodynamic instability, resting tachypnea); * acute exacerbations in the month prior to enrollment; * cognitive impairment such that participation in rehabilitation activities is impaired (Mini Mental State Examination \< 24); * cardiovascular decompensation NYHA (New York Heart Association) class III and IV; * major cardiac arrhythmias; * active solid or hematologic neoplasms; * recent myocardial infarction (\< 6 months); * orthopedic clinical conditions that interfere with exercise.

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Conditions

The condition(s) this trial relates to.

cerebral palsy chronic obstructive pulmonary disease COPD, severe early onset stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cerebral palsy COPD Healthy volunteer Stroke

Contacts and locations

Locations

  • CNR-STIIMA - Lecco

    Lecco, Lecco, 23900, Italy

  • IRCCS E. Medea

    Bosisio Parini, LC, Italy

  • IRCCS INRCA Casatenovo

    Casatenovo, LC, Italy

  • Villa Beretta Rehabilitation Clinic - Valduce Hospital

    Costa Masnaga, LC, Italy

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