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Mind-Body moves: yoga, walking, and meditation put to the test for better sleep

NCT ID NCT05789212

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed Phase 2 trial tested whether a personalized mind-body program could improve sleep in 60 women aged 40–60 who work in healthcare and report short sleep. Participants tried 30-minute sessions of mindfulness, yoga, and guided walking in different orders over 12 weeks. Sleep was tracked with Fitbits and surveys. The goal was to see if these activities could add meaningful minutes to nightly sleep.

What this could mean

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

Active substance
mindfulness, yoga, and guided walking
What this could lead to
If it works, this could offer a simple, drug-free way to improve sleep in busy healthcare workers.
What could go wrong
This is a small pilot study with only 60 participants, so results may not apply to everyone. The effect on sleep may be modest or hard to separate from natural changes over time.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

60 people

The number who actually took part.

Started

May 2023

Finished

Jan 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

40 to 60 years

Sex

Female participants only

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: * Women (biological sex at birth) * Age 40-60 years old * Northwell employee/affiliate * Self-reported history of short sleep duration (\<7h per 24-h period) for at least 3 months * After 2-week run-in, Fitbit-verified short sleep duration and ≥80% adherence of Fitbit wear and survey submission * Self-report of perceived stress ≥18 using the Perceived Stress Scale (PSS) * Access to and capable of using a smartphone * Can regularly wear a Fitbit device Exclusion Criteria: * Men (biological sex at birth) * Age \< 40 or \>60 years old * Women who are pregnant * Not a Northwell employee/affiliate * No history of short sleep duration or non-adherent to the Fitbit wear and survey submission * Self-report of perceived stress \<18 using the Perceived Stress Scale (PSS) * Does not own or cannot regularly access a smartphone * Cannot regularly wear a Fitbit device * Unable to complete the study due to cognitive impairment, severe medical or mental illness, or active/prior substance abuse * Planned surgeries 6 months from study start date * Participants who have been previously told by a doctor/clinician they have mobility limiting health conditions and/or to not engage in walking 30 minutes, three times per week or yoga

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Conditions

The condition(s) this trial relates to.

anxiety disorder Depression insomnia Sleep Deprivation

As listed by the trial registrant

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

Contacts and locations

Locations

  • Institute of Health System Science

    New York, New York, 10022, United States