Prehabilitation before gynecologic surgery may speed recovery
NCT ID NCT07188662
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether a multimodal prehabilitation program (exercise, nutrition, and education before surgery) could improve outcomes for 140 women undergoing gynecologic cancer surgery. The program was combined with enhanced recovery after surgery (ERAS) care. Researchers measured complications, pain, and hospital stay length within 30 days after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multimodal prehabilitation program (exercise, nutrition, and education before surgery)
- What this could lead to
- If it works, this program could help women recover faster and with fewer complications after gynecologic cancer surgery.
- What could go wrong
- This is a small, completed study with no phase designation, so results may not apply to all patients. The program requires extra time and effort before surgery.
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
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140 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Jul 2025
- 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 to 70 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Newly diagnosed woman with gynecologic cancer by imaging \&histopathology * Accept participation in the study. Exclusion Criteria: * Patient with advanced and metastatic stage * Patient who received neoadjuvant chemotherapy * Patient who have psychological disorder such as suicidal attempt * Patient who have cerebral stroke, hemiplegia or paralyses
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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.
Contacts and locations
Locations
-
Woman's Health Hospital
Asyut, Egypt
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Other studies related to the condition(s) this trial covers.
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