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Turkish Version of the QoR-15 for Emergency Laparotomy

Validation of the Turkish Version of QoR-15 (QoR-15T) Scale for Emergency Laparotomy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05794269
Acronym
QoR-15T-EL
Enrollment
100
Registered
2023-04-03
Start date
2023-02-01
Completion date
2023-08-01
Last updated
2023-04-04

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

Conditions

Anesthesia, Postoperative Complications, Quality of Life, Surgery

Brief summary

Patient perceived quality of recovery is an important outcome after surgery and should be measured in clinical trials. The QoR-15 was designed to measure quality of recovery postoperatively. It provided an efficient evaluation of the postoperative quality of recovery. The primary objectives of this study is validate the Turkish version of QoR-15 questionnaire for emergency laparotomy. The investigators will test its validity, reliability, responsiveness, and clinical acceptability and feasibility, with patients emergency laparotomy, in the University of Health Sciences, Gülhane Education and Training Hospital Ankara, Türkiye.

Detailed description

Recovery from surgery is a complex process that can vary depending on the patient and the anesthesia used. Most clinical studies are interested in reducing perioperative morbidity and mortality, but few evaluate the overall recovery process. The QoR-15 questionnaire assess recovery after elective surgery. A Turkish translation of the QoR-15 score has been validated for use in scheduled surgery. This scale, regardless of the language in which it is translated, has been developed and validated in patients who have undergone scheduled surgery. Until now, no validated scoring tool has been available to assess recovery after emergency laparotomy.

Interventions

OTHERTQoR-15 questionnaire

The TQoR-15 questionnaire (Turkish version) consists of 15 questions concerning five domains (the patient's feelings, comfort, pain, dependence on the health care team and psychological well-being). Two to three minutes are required to complete all the questions. If the patient is not able to read the questionnaire himself, a third person can ask the patient the questions orally. Each item is scored from 0 to 10 and the total score is the sum of the score obtained for each item, i.e. a score from 0 to 150.

Sponsors

Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* ≥ 18 years old, * Turkish speaking, * Admitted for any type of emergency laparotomy (time to surgery \< 72 hours) * Able to answer the questionnaire at hospital admission, alone or with the help of a third party * And agreeing to participate in the study.

Exclusion criteria

* Patients with psychiatric or neurological pathologies that compromise cooperation with the protocol, * Patients admitted for revision surgery, * aged \< 18 years old * not agreed to provide written informed consent to participate

Design outcomes

Primary

MeasureTime frameDescription
Validity of TQoR-15 questionnaire (24 hours)At 24 hours after surgeryEvaluate the validity of the Turkish version of the QoR-15 to assess immediate postoperative recovery after emergency laparotomy (at 24 hours)
Validity of TQoR-15 questionnaire (72 hours)At 72 hours after surgeryEvaluate the validity of the Turkish version of the QoR-15 to assess immediate postoperative recovery after emergency laparotomy (at 72 hours)

Secondary

MeasureTime frameDescription
Minimal important differenceAt 24 and 72 hours after surgeryEstimate minimal important difference from the TQoR-15 questionnaire in the emergency laparotomy population.

Countries

Turkey (Türkiye)

Contacts

Primary ContactUmut KARA
drumutkara@gmail.com+905339392399
Backup ContactSerkan ŞENKAL
senkalserkan@gmail.com+905338142614

Outcome results

None listed

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