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Mindfulness may tame the Body's stress fire after repeated floods

NCT ID NCT07790055

Symptom relief Sponsor: Natalia Dewi Wardani, MD Source: ClinicalTrials.gov ↗

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 27, 2026 · Last updated Sep 02, 2026 · Updated 3 times

Summary

This trial tests whether an 8-day mindfulness body scan can reduce stress and inflammation in people who have survived repeated tidal flooding. Researchers will measure blood markers like IL-6, TNF-α, CRP, and cortisol, along with questionnaires on depression, anxiety, sleep, and quality of life. Participants are adults from Sayung District, Demak, who are registered at a local health center. Half will receive the mindfulness training, and the other half will get standard health monitoring.

What this could mean

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

Active substance
Mindfulness Body Scan Training, an 8-day structured mind-body exercise
What this could lead to
If it works, this could offer a simple, drug-free way to ease stress and inflammation for people living through repeated disasters.
What could go wrong
The trial is small and short, and it focuses on one community, so results may not apply broadly. Mindfulness may not change blood markers of inflammation in everyone.

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 75 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

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

18 to 60 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 18 years or older. * Resident of Sayung District, Demak Regency, affected by tidal flooding (rob). * Registered patient at Sayung 1 Primary Health Center. * Capable of providing written informed consent and participating in the intervention sessions. Exclusion Criteria: * Severe cognitive impairment, active psychosis, or severe psychiatric conditions preventing participation. * Uncontrolled systemic autoimmune or inflammatory diseases. * Current use of long-term systemic corticosteroid or immunosuppressive therapy. * Inability to complete questionnaires or follow basic mindfulness instructions.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Depression Inflammation inflammatory disease major depressive disorder Stress, Psychological

As listed by the trial registrant

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

Anxiety Depression - major depressive disorder Disaster Inflammation Psychological stress

How to take part

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

  1. The places running it

    1 site. 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.

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  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

  • Puskesmas Sayung 1

    Demak, Central Java, Indonesia

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