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The Effect of Preoperative Patient Education on Early Ambulation in Gynecological Surgery

A

Aydin Adnan Menderes University

Status

Completed

Conditions

Surgery
Gynecologic Nursing
Nurse's Role

Treatments

Behavioral: Preoperative patient education

Study type

Interventional

Funder types

Other

Identifiers

NCT05845086
Postoperative ambulation

Details and patient eligibility

About

This study was planned as a randomized controlled study to test the effect of multimedia supported patient education reinforced with the "teach back" method in the preoperative period on postoperative mobilization in women who underwent gynecological oncology surgery.

Full description

Mobilization; It is defined as "standing up, walking, being able to move and walking around, especially after the operation, when the patient stands up and walks around". Postoperative mobilization is a basic human need and one of the basic principles of nursing care. In the postoperative period, with the delay of mobilization, the patient's insulin resistance increases, muscle weakness and muscle mass loss occur, problems in pulmonary functions are experienced and the risk of thromboembolism increases. On the other hand, there is a significant relationship between increasing postoperative mobilization and postoperative recovery. It has been reported that day mobilization is significantly associated with successful surgical outcome and postoperative recovery (such as early return of bowel movements, shorter initiation of oral intake, shorter hospital stay).

Early mobilization after gynecological oncology surgeries is an important component of nursing care during the surgical process and one of the basic responsibilities of the surgical nurse. Within the scope of this responsibility, nurses should comprehensively evaluate patients physiologically and psychologically in the preoperative period, follow current evidence-based practices, and plan the nursing care process based on these practices in accordance with the clinical condition of the patient. It is reported that by following evidence-based practices in the treatment and care practices of patients in the postoperative period, the postoperative recovery process will be accelerated, the complications seen will be reduced, the hospital stay will be shortened, mortality and morbidity rates will be reduced, and patient satisfaction will be increased.

In this study, a systematic review and meta-analysis study was carried out to identify evidence-based interventions used to increase early postoperative mobilization and search PubMed, EBSCO (Medline, CINAHL), Web of Science, Cochrane, ClinicalTrials.gov and Turkey national databases (Dergipark, Turkey). Clinics, Turkmedline, and the National Thesis Center, Cochrane Library and TUBITAK Ulakbim databases were used in the last 20 years (01.01.2002-31.12.2022). Systematic reviews and meta-analyses published in Turkish and English are limited to observational studies, non-randomized and randomized controlled studies. Keywords were created according to the research question. MeSH (Medical Subject Headings) was used for English keywords, and Science Words of Turkey (SWT) was used to create Turkish equivalents of English keywords. The keywords used in the search were determined as "early ambulation" OR "early mobilization". The English keywords were determined as "Gynecologic Surgery" OR "Gynecological Surgery" OR "Gynecologic Surgical Procedure" OR "Gynecological Surgical Procedures" AND "Accelerated Ambulation" OR "Early Ambulation" OR "Early Mobilization". As a result of the screening, 6 studies that met the inclusion criteria and 2 interventions that were effective in increasing postoperative mobilization after gynecological oncology surgery were identified:

  • Preoperative patient education,
  • Exercise protocols. According to these results, it was decided to test the preoperative patient education in a randomized controlled experimental phase, considering the fact that this study is a doctoral thesis, the time limitation of the study, and the feasibility of the intervention.

Enrollment

112 patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having elective surgery
  • Be conscious
  • Having undergone gynecological oncological (vulva-vaginal cancer, ovarian cancer, cervical cancer, fallopian tube cancer, endometrial cancer) surgery
  • Absence of mental and physical problems (such as Alzheimer's disease, dementia, orthopedic problems and limb amputation) that prevent early mobilization
  • Having normal blood pressure and heart rate
  • Being in ASA I, II and III classification
  • Absence of abnormal findings at the incision site
  • Have a phone number where you can be reached
  • Permission of the physician (As the physician may recommend absolute bed rest to the patient in some cases in accordance with the clinical picture of the patients, the patient will not be included in the study in the presence of such a recommendation)

Exclusion criteria

  • Being diagnosed with a neurological and/or psychiatric disorder
  • Having a disability related to mobility
  • Those with delirium in the postoperative period
  • Patients with cardiac problems
  • Patients with a history of diagnosed venous thrombosis
  • Have had surgery in the last 1 month those who are pregnant
  • Patients with a body temperature of 38.5 and above in the perioperative period
  • Don't be intubated
  • Lack of knowledge that he has been diagnosed with cancer (the case that the diagnosis is hidden from the patient)
  • Using an assistive device for mobility
  • Physician's written bed rest instruction
  • Presence of abnormal finding in the surgical field
  • Presence of a pacemaker
  • Presence of respiratory diseases

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

112 participants in 2 patient groups

Intervention group (Preoperative patient education)
Experimental group
Description:
In addition to the usual care provided by the nurses, the intervention group will be provided with multimedia-supported written and verbal pre-operative patient training, reinforced by the teach-back method, created according to the literature.
Treatment:
Behavioral: Preoperative patient education
Control group (Usual care)
No Intervention group
Description:
The control group continued to receive the usual care

Trial contacts and locations

1

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Central trial contact

Ezgi Arslan, PhD Students

Data sourced from clinicaltrials.gov

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