A structured education program may ease recovery after hysterectomy — a trial puts it to the test
NCT ID NCT07721727
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This trial tests whether a structured education program, based on the Roy Adaptation Model, can improve adaptation, self-esteem, and quality of life in women who have had a hysterectomy. About 110 premenopausal women who have undergone the surgery will be randomly assigned to receive either the education program or routine care. Researchers will measure changes in adaptation, self-esteem, and quality of life over eight weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a structured education program based on the Roy Adaptation Model for women after hysterectomy
- What this could lead to
- If effective, this program could offer a simple, low-cost way to help women adjust emotionally and physically after hysterectomy.
- What could go wrong
- This is a small, early-stage trial. The program may not significantly improve outcomes over standard care, and results may not apply to all women.
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 108 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 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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18 years and older
- Sex
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Female participants only
- 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: * Women who have completed at least primary school education. Premenopausal women who have undergone hysterectomy. Have access to the internet and possess a device (smartphone, tablet, or computer) capable of participating in online education sessions. Have an adequate level of health literacy to understand the educational materials, access online information, and follow the intervention. Be sexually active. Exclusion Criteria: * Diagnosed with a sleep disorder. Have a physical and/or mental disability. Have communication difficulties (e.g., speech, language, comprehension, or cognitive impairment). Have a diagnosis of cancer. Currently receiving hormone therapy.
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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