Pre-Operative Prehabilitation Program Women With Gynecological Cancer

Istanbul University - Cerrahpasa (IUC)

Status: Not yet enrolling

Conditions: Gynecologic Cancer; Prehabilitation

Treatments: Other: Prehabilition program

Study type: Interventional

Funder types: Other

Identifiers

NCT06176274

IstanbulUC-LEE-HE-01

Details and patient eligibility

About

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.

Full description

The aim of prehabilitation programs is to eliminate intraoperative complications by increasing the functional capacity and metabolic reserves of patients before surgical treatment and to accelerate recovery in the postoperative period. In addition, it helps the patient to maximize the existing capacity of the patient before the surgery, to know what will happen at each stage of the treatment to be applied to the patient, to feel better physically and spiritually and to understand the roles and responsibilities of the individual care of the patient, as well as making a significant contribution to the positive results of the operation. It is to provide exercise, psychological support, nutritional counseling and optimization of the underlying conditions by stopping negative health behaviors. There are non-eliminable criteria such as age, gender, comorbid diseases before surgery, as well as modifiable factors such as the regulation of the patients nutrition, ensuring psychological well-being, quitting smoking. In particular, some factors directly affect the state of well-being during the perioperative period. Thus, surgeries become safer.As a practice, the prehabilitation program (according to the surgery program) is planned in the preoperative period between 2-4 weeks Dec. Participants who do not comply with the program will be excluded from the sample

Enrollment: 50 estimated patients

Sex: Female

Ages: 50+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

50 participants in 2 patient groups

the experimental group

Experimental group

Description:

a prehabilitation program will be applied before the surgery.

Treatment:

Other: Prehabilition program

The Control Group

No Intervention group

Description:

he will receive standard nursing care procedure.