Perioperative Anxiety Risk Factors in Parents of Children Undergoing Thoracic Surgery

NCT05752708 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 123

Last updated 2025-04-15

No results posted yet for this study

Summary

Risk factors associated with perioperative anxiety in parents of pediatric patients undergoing thoracic surgery are unknown. It is therefore necessary to identify them in order to better understand, above all, modifiable factors. This will allow the implementation of psychological interventions tailored to the individual needs of parents to strengthen their coping mechanisms before surgery, and thus facilitate the recovery process of their children after surgery.

The purpose of the study is:

1. assessment of the level of anxiety experienced by parents before and after thoracic surgery,
2. assessment of risk factors for parents' perioperative anxiety,
3. assessment of the relationship between parents' perioperative anxiety and satisfaction with postoperative analgesia

Conditions

  • Anxiety State
  • Anxiety Postoperative
  • Parents
  • Surgery
  • Thoracic
  • Satisfaction

Interventions

DIAGNOSTIC_TEST

Diagnostic Test

Evaluation of perioperative anxiety in parents of children undergoing thoracic surgery using standardized tests: The Amsterdam Preoperative Anxiety and Information Scale (APAIS), the State-Trait Anxiety Inventory (STAI).

Sponsors & Collaborators

  • National Institute for Tuberculosis and Lung Diseases, Poland

    lead OTHER

Principal Investigators

  • Lucyna Tomaszek, PhD · National Institute for Tuberculosis and Lung Diseases, Poland

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-16
Primary Completion
2025-09-30
Completion
2025-09-30

Countries

  • Poland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05752708 on ClinicalTrials.gov