Mind over scalpel: guided imagery tested for bariatric recovery
NCT ID NCT07157826
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether listening to a guided imagery recording can reduce pain, anxiety, fear, and stress, and improve sleep quality in people recovering from bariatric surgery. Seventy adults will be randomly assigned to either listen to the recording or receive standard care. Researchers will measure changes using questionnaires and check vital signs and cortisol levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- guided imagery audio recording
- What this could lead to
- If it works, this could offer a simple, drug-free way to help bariatric surgery patients feel less pain and anxiety and sleep better after their operation.
- What could go wrong
- This is a small, early-stage trial with only 70 people, so results may not apply to everyone. The effect of guided imagery can vary a lot from person to person.
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
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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
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2025
An estimate. Start dates often move.
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Willingness to participate in the study * Ability to communicate verbally * No history of psychiatric disorders * Undergoing laparoscopic bariatric surgery using the Sleeve Gastrectomy method * Ability to use a smartphone * No prior experience with guided imagery intervention Exclusion Criteria: \-
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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Atatürk University
Erzurum, Palandöken, 25000, Turkey (Türkiye)
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