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Multimodal Prehabilitation Program for Women Undergoing Gynecologic Oncology Surgery

A

Assiut University

Status

Completed

Conditions

Gynecologic Oncology Patient

Treatments

Procedure: group (B) Prehabilitation care combine with ERAS post-operative care

Study type

Interventional

Funder types

Other

Identifiers

NCT07188662
MMPPGOS

Details and patient eligibility

About

The goal of this clinical trial is to evaluate the role of multimodal Prehabilitation program on improve surgical outcomes after gynecological oncology surgery.

Full description

Multimodal prehabilitation program focused on improving woman physical and psychological wellbeing before gynecological oncology surgery. Multimodal prehabilitation refers to a combination of preoperative interventions targeting physical, nutritional, psychological, and medical optimization. This program included various element such preoperative physical exercise, nutritional support, psychological counselling, social support and education about surgical processes. Multimodal Prehabilitation programs play an important role in improving surgical outcomes after gynecological oncology surgery.

Enrollment

140 patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

140 participants in 2 patient groups

Conventional group
No Intervention group
Description:
Conventional group (woman received hospital care at previous year as a retrospective sample to prevent risk of bias) equal 70 woman
Prehabilitation group
Experimental group
Description:
Prehabilitation group (woman who will receive prehabilitation care combine with ERAS post-operative care as a prospective sample) equal 70 woman
Treatment:
Procedure: group (B) Prehabilitation care combine with ERAS post-operative care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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