Clinical trial · Interventional
Pre-Operative Prehabilitation Program Women With Gynecological Cancer
The Effect of Pre-Operative Prehabilitation Program on Postoperative Recovery in Women With Gynecological Cancer
NCT06176274CI-TRIAL-00072368unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this study is to determine the effect of the prehabilitation program applied to postmenopausal women diagnosed with gynecological cancer before surgery on postoperative recovery, planned as a randomized study with an experimental design with a pre-test post-test control group.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gynecologic Cancer | Malignant Female Reproductive System Neoplasm | ALIAS | 0.90 |
| Prehabilitation | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Prehabilition program | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- the experimental group
- description
- a prehabilitation program will be applied before the surgery.
- interventionNames
- Other: Prehabilition program
- type
- NO_INTERVENTION
- label
- The Control Group
- description
- he will receive standard nursing care procedure.
Primary outcomes (4)
- measure
- the Quality of Recovery QoR-15
- timeFrame
- 6 weeks
- description
- The scale is based on the assumption that the higher the score, the better the quality of improvement when measuring between 0 and 150 points. The scale is based on the assumption that the higher the score, the better the quality of Deceleration.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 50 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who are not stage 4 in preoperative evaluation * Who volunteered to participate in the study * 6 months have passed since the last treatment (Chemoretapy, Radiotherapy) * Women who do not have Turkish literacy problems * Women aged 50 and older who are in the postmenopausal period * Patients who are scheduled for abdominal surgery Exclusion Criteria: * High-risk comorbid diseases such as COPD, heart failure * Physical and mental conditions that will interfere with nutrition and exercise * Those with orthopedic and neuromuscular diseases * Those who are scheduled for surgery by laparoscopic/laparotomic method * Those who cannot adapt to the program during the preoperative period * Women who are too depressed during preoperative evaluation
References
Publications (0)
Data not yet available
No reference posted for this study.