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Can High-Intensity workouts boost stroke recovery?

NCT ID NCT07274748

Symptom relief Sponsor: Riphah International University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looks at two types of exercise—high intensity interval training and intermittent functional training—to see which one better helps stroke survivors improve their heart fitness, physical abilities, and thinking skills. About 52 adults aged 50-75 who had a stroke at least 6 months ago will take part. The goal is to find the most effective way to support recovery and quality of life after a stroke.

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

About 52 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2025

Expected to finish

May 2026

An estimate. End dates often move.

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

50 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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:• Age 50-75 years * Both male and female stroke patients are included. * Unilateral stroke experienced greater than 6 months prior to enrollment * NIHSS: National Institute of Health Stroke Scale (a score of 5 to 15 represents a moderate stroke) * Able to walk 10 minutes over ground with assistive devices as needed without physical assistance * Able to walk 3 minutes on the treadmill at greater than 0.3 mph with no aerobic exercise contraindications. * Stable cardiovascular condition (American Heart Association class B) * Not currently participating in formal rehabilitation. Exclusion Criteria:• Significant resting ECG abnormalities * Diagnosed cardiovascular abnormalities * Evidence of myocardial ischemia or significant arrhythmia on stress test hospitalization for cardiac or pulmonary disease within the previous 3 months, pacemaker or implanted defibrillator * Lower extremity (LE) claudication * Unable to communicate with investigators or correctly answer consent comprehension questions * Severe LE spasticity (Ashworth scale score \>2) * LE weight-bearing pain \>4/10 on a visual analog scale.

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

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

Stroke

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Riphah International University

    NOT_YET_RECRUITING

    Daska Kalan, Punjab Province, 51010, Pakistan

  • Riphah International University

    RECRUITING

    Daska Kalan, Punjab Province, 51010, Pakistan

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