Multimodal Prehabilitation Program for Women Undergoing Gynecologic Oncology Surgery

NCT ID: NCT07188662

Last Updated: 2025-09-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 140 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-04-23
• Study Completion Date: 2025-07-23

Brief Summary

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

Detailed 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.

Conditions

Gynecologic Oncology Patient

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Conventional group

Conventional group (woman received hospital care at previous year as a retrospective sample to prevent risk of bias) equal 70 woman

Group Type: NO_INTERVENTION

No interventions assigned to this group

Prehabilitation group

Prehabilitation group (woman who will receive prehabilitation care combine with ERAS post-operative care as a prospective sample) equal 70 woman

Group Type: EXPERIMENTAL

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

Intervention Type: PROCEDURE

intervention will includes receiving prehabilitation care combine with ERAS post-operative care.

Interventions

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

intervention will includes receiving prehabilitation care combine with ERAS post-operative care.

Intervention Type: PROCEDURE

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Assiut University

OTHER

Sponsor Role: lead

Responsible Party

Aya M. Abdelhafez

lecturer of maternity, gynecological and obstetric nursing

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Aziza M Mohammed, Head nurse

Role: STUDY_CHAIR

Woman's Health Hospital, Assiut University, Egypt

Locations

Woman's Health Hospital

Asyut, , Egypt

Countries

Egypt

Other Identifiers

MMPPGOS

Identifier Type: -

Identifier Source: org_study_id