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ObsQoR-11: Quality of Postpartum Cesarean Recovery Score Validity Reliability

Sponsor
Ondokuz Mayıs University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05373563
Collaborator
(none)
1
Enrollment
1
Location
2.3
Anticipated Duration (Months)
0.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: cesarean section women

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 Design

Study Type:
Observational
Anticipated Enrollment :
1 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Quality of Postpartum Cesarean Recovery Score Validity Reliability
Actual Study Start Date :
Jul 24, 2022
Anticipated Primary Completion Date :
Sep 5, 2022
Anticipated Study Completion Date :
Oct 2, 2022

Outcome Measures

Primary Outcome Measures

  1. Quality of Postpartum Cesarean Recovery Score validity reliability [July 2022-October 2022]

    Measuring early recovery after cesarean section

  2. obstetric qualityof- recovery score (ObsQoR-11) [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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsun Health Directorate Samsun Black Sea Turkey 55060

Sponsors and Collaborators

  • Ondokuz Mayıs University

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ümmühan kılıç, Principal Investigator, Ondokuz Mayıs University
ClinicalTrials.gov Identifier:
NCT05373563
Other Study ID Numbers:
  • SAMSUN HEALTH DİRECTORATE
First Posted:
May 13, 2022
Last Update Posted:
Aug 5, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 5, 2022