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Impact of Preoperative Sleep Quality and Anxiety on Postoperative Outcomes in Abdominal Gynecologic Cancer Surgery

Impact of Preoperative Sleep Quality and Anxiety on Postoperative Outcomes in Abdominal Gynecologic Cancer Surgery: A Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07036549
Enrollment
72
Registered
2025-06-25
Start date
2025-02-15
Completion date
2025-05-15
Last updated
2025-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecologic Neoplasms

Keywords

Sleep Quality, Anxiety, Postoperative Pain, Gynecologic Cancer Surgery, Preoperative Assessment, Patient Outcomes, Psychological Stress, Hospital Stay

Brief summary

This prospective observational study aims to evaluate the effects of preoperative sleep quality and anxiety levels on postoperative outcomes in patients undergoing abdominal gynecologic cancer surgery. A total of 72 patients were included and assessed using the Pittsburgh Sleep Quality Index (PSQI) and the Beck Anxiety Inventory (BAI) prior to surgery. Postoperative outcomes including pain scores (measured by the Numeric Rating Scale), complication rates, additional analgesic use, and length of hospital stay were recorded. The findings suggest that poor sleep quality and high anxiety levels prior to surgery are significantly associated with higher postoperative pain, increased complication rates, and prolonged hospital stay. These results emphasize the importance of preoperative psychological evaluation and supportive interventions to improve perioperative care in gynecologic oncology.

Detailed description

This prospective observational study was conducted between February and May 2025 at a tertiary gynecologic oncology center. The aim was to evaluate the association between preoperative sleep quality and anxiety levels with postoperative outcomes in patients undergoing open abdominal surgery for gynecologic cancer. Eligible participants were women aged 18 years or older who were scheduled for elective laparotomy with general anesthesia. Patients with psychiatric disorders, major neurological conditions, or incomplete postoperative data were excluded. Sleep quality was assessed preoperatively using the Pittsburgh Sleep Quality Index (PSQI), and anxiety was measured using the Beck Anxiety Inventory (BAI). Patients with a PSQI score ≥5 were classified as having poor sleep quality, and those with BAI scores ≥16 were classified as having high anxiety. Postoperative pain was evaluated using the Numeric Rating Scale (NRS) at 0, 4, 8, 12, and 24 hours after surgery. Additional analgesic requirements, early postoperative complications (e.g., surgical site infection, ileus, nausea-vomiting, atelectasis), and length of hospital stay were recorded. The study also examined potential psychosocial contributors such as mobile phone use during sleep, internet-based health information seeking, and patients' satisfaction with preoperative counseling using a structured Likert scale. All data were collected via face-to-face interviews and hospital records. Statistical analyses included Mann-Whitney U test, chi-square test, and Spearman correlation coefficients. The study was approved by the Institutional Ethics Committee (Approval No: 2025/38), and all participants provided written informed consent.

Interventions

None listed

Sponsors

Izmir City Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female patients aged ≥18 years * Diagnosed with gynecologic malignancy * Scheduled for elective abdominal surgery (laparotomy) * Able to provide informed consent * Completed preoperative sleep and anxiety assessments

Exclusion criteria

* History of psychiatric or cognitive disorders interfering with questionnaire participation * Emergency surgical procedures * Incomplete follow-up data within 30 days postoperatively * Patients admitted for inpatient observation prior to surgery * Major previous pelvic surgery

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Pain Score (Numeric Rating Scale)Postoperative Day 1 (within 24 hours after surgery)Postoperative pain will be assessed using the Numeric Rating Scale (NRS) at 0, 4, 8, 12, and 24 hours after surgery. Higher scores indicate greater pain intensity.

Secondary

MeasureTime frameDescription
Postoperative Complication RateUp to 30 days after surgeryIncidence of postoperative complications including surgical site infection, ileus, nausea-vomiting, and atelectasis recorded within 30 days after surgery.
Additional Analgesic RequirementPostoperative Day 1 (within 24 hours after surgery)Requirement for rescue analgesics (non-protocol) within the first 24 hours postoperatively.
Length of Hospital StayFrom day of surgery until discharge (mean: 4.2 days)Duration of postoperative hospitalization measured in days from the day of surgery until the day of discharge, based on electronic medical records.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026