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Tiny exercise 'Snacks' after meals may tame blood sugar spikes

NCT ID NCT07620886

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether light physical activity after meals can improve blood sugar levels in adults with metabolic syndrome and prediabetes. Twenty-five participants will try three routines in random order: sitting, a 15-minute walk, or brief resistance exercises like squats every 20 minutes after a meal. The goal is to see if these simple activities help lower average blood sugar over 24 hours.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
postprandial walking and brief resistance exercise snacks
What this could lead to
If it works, this could point toward a simple, drug-free way to manage blood sugar after meals for people with prediabetes.
What could go wrong
This is a very small, early-stage trial with only 25 participants, so results may not apply to everyone. The exercises are short and may not produce lasting changes.

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 25 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Oct 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

40 to 65 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: * Inclusion Criteria: * Adults aged 40 to 65 years * Presence of metabolic syndrome * Fasting glucose of 100 mg/dL or higher or HbA1c of 5.7% or higher * Not regularly engaged in structured exercise training, defined as less than 150 minutes per week during the past year * Able to consume the standardized study meals * Able to wear a continuous glucose monitor and a chest strap heart rate monitor * Able to provide written informed consent Exclusion Criteria: * History of major cardiovascular, cerebrovascular, respiratory, renal, hepatic, neurological, or other severe medical conditions that may affect study participation. * Uncontrolled hypertension, defined as systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg. * Current use of medications associated with a high risk of hypoglycemia, such as insulin or sulfonylureas. * Initiation or dose change of insulin or oral glucose-lowering medications within the past 3 months. * Initiation or dose change of medications for hypertension, dyslipidemia, or diabetes within the past 3 months. * Musculoskeletal, neurological, or orthopedic conditions that limit safe participation in walking or body-weight resistance exercise, including severe knee, hip, back, or ankle pain. * Regular participation in moderate-to-vigorous exercise of 150 minutes or more per week during the past year. * Difficulty consuming the standardized study meals, including food allergy, dietary restrictions, or severe gastrointestinal symptoms. * Difficulty wearing a continuous glucose monitor or history of severe skin irritation or allergy to adhesive sensors. * Difficulty wearing a chest strap heart rate monitor or skin problems at the chest strap site. * Pregnancy or planned pregnancy. * Acute illness, infection, surgery, or hospitalization within the past month. * Current participation in another interventional study. * Any condition judged by the investigator to make participation unsafe or inappropriate. Exclusion Criteria: \-

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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