Quality of Postpartum Cesarean Recovery Score Validity Reliability (ObsQoR-11)

January 25, 2023 updated by: ümmühan kılıç, Ondokuz Mayıs University
In order to provide the best care of patients after cesarean section, to help solve all their biopsychosocial problems in the recovery process, and to shorten the hospitalization period, it should be measured with appropriate measurement tools for various evaluations. The Scale of Post-cesarean Healing Quality You will provide in adapting the ObsQoR-11 questionnaire to Turkish.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In order to provide the best care of patients after cesarean section, to help solve all their biopsychosocial problems in the recovery process, and to shorten the hospitalization period, it should be measured with appropriate measurement tools for various evaluations. We will provide the Scale of Post-Cesarean Healing Quality in adapting the ObsQoR-11 questionnaire to Turkish.It is important to define well the recovery after cesarean section.

Study Type

Observational

Enrollment (Actual)

1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • Black Sea
      • Samsun, Black Sea, Turkey, 55060
        • Samsun Health Directorate

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Study study of 18 patients using large cesarean section.

Description

Inclusion Criteria:

  • Must be Over 18 age,
  • Must be literate women,
  • Must be no neurological disease

Exclusion Criteria:

  • Must be unwilling to participate in the study
  • Must be under 18 years old women

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of Postpartum Cesarean Recovery Score validity reliability
Time Frame: July 2022-October 2022
Measuring early recovery after cesarean section
July 2022-October 2022
obstetric qualityof- recovery score (ObsQoR-11)
Time Frame: About six mount

Women were approached while in the postnatal ward 24 h after CS and asked to complete the ObsQoR-11K questionnaire and to choose a point in the 100-mm numeric rating scale (NRS) to evaluate global health status. Women rated each recovery item using an 11-point numerical Likert scale (0 = strongly negative; 10 = strongly positive).

Global health status was measured using NRS indicated by a 100 mm line (0 = 'worst imaginable health status' and 'sad' face; 100 = 'best imaginable health status' and 'happy' face).
About six mount

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Ondokuz Mayıs University

Investigators

  • Principal Investigator: Dilek Kıymaz,, PhD, Samsun Provincial Health Directorate
  • Study Chair: Esra Saraçoğlu, PhD, Samsun Provincial Health Directorate

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 24, 2022

Primary Completion (Actual)

September 5, 2022

Study Completion (Actual)

October 2, 2022

Study Registration Dates

First Submitted

April 22, 2022

First Submitted That Met QC Criteria

May 9, 2022

First Posted (Actual)

May 13, 2022

Study Record Updates

Last Update Posted (Estimate)

January 26, 2023

Last Update Submitted That Met QC Criteria

January 25, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • SAMSUN HEALTH DİRECTORATE

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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