CClinicalTrials.gg
Status unknownNCT04389515Updated Sep 2, 2020

Postoperative Recovery Index, Patient Expectations and Satisfaction With Prenatal Care Instrument in Pregnant Patients With COVID-19

An observational study in COVID-19, Prenatal Care and Postoperative Care, sponsored by Kanuni Sultan Suleyman Training and Research Hospital. Status unknown at 1 site in Turkey. Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-09-02.

Sponsored by Kanuni Sultan Suleyman Training and Research Hospital · Observational

The sponsor has not verified this record recently (last verified Aug 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
75
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The aim of this study is to provide optimum care to postoperative patients diagnosed with COVID-19 (after cesarean) and to help them with recovery, to determine and assist the expectation and satisfaction of pregnant women with COVID-19 regarding prenatal care.

02

Conditions studied

  • COVID-19
  • Prenatal Care
  • Postoperative Care

Browse trials for

Keywords

  • COVID-19
  • Prenatal Care
  • Postoperative Care
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's planned enrollment of 75 is below the median of 261 across 3,136 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

Kanuni Sultan Suleyman Training and Research Hospital is the lead sponsor of 216 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

As the patient group, two groups of 75 persons, each of whom are between the ages of 18-45 and who are diagnosed with COVID-19 in reproductive age and healthy pregnant women, will be selected. Patients diagnosed with COVID-19 giving birth with cesarean at term and patients who are followed up with COVID-19 diagnosis before the prenatal period will be selected.

Inclusion criteria

  • Pregnant patients with COVID-19

Exclusion criteria

Exclusion Criteria:

  • Patient giving Preterm Labor
05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
75 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Evaluation of pregnant women diagnosed with COVID-19 with "Post-operative Recovery Index" and "Prenatal Care Satisfaction and Patient Expectations Scale"

    The benefit we expect from the study is to be able to provide optimum care to postoperative patients (after cesarean) diagnosed with COVID-19 and to help them with recovery, to identify and assist the expectation and satisfaction of pregnant women with COVID-19 regarding prenatal care.

    Time frame: 3 Months

Secondary outcomes

  1. Evaluation of pregnant women diagnosed with COVID-19 with "Post-operative Recovery Index" and "Prenatal Care Satisfaction and Patient Expectations Scale"

    To determine the differences between healthy pregnant women in the control group and pregnant women diagnosed with COVID-19 in the study group in terms of postoperative care and prenatal care expectations.

    Time frame: 3 Months

07

Study locations

1 of 1 sites recruiting
  • Kanuni Sultan Suleyman Training and Research Hospital
    Istanbul, Halkali 34307, Turkey
    Recruiting
08

References and documents

Publications

  • Omar MA, Schiffman RF, Bingham CR. Development and testing of the patient expectations and satisfaction with prenatal care instrument. Res Nurs Health. 2001 Jun;24(3):218-29. doi: 10.1002/nur.1024. PubMed 11526620 ↗
  • Cengiz H, Aygin D. Validity and reliability study of the Turkish version of the Postoperative Recovery Index of patients undergoing surgical intervention. Turk J Med Sci. 2019 Apr 18;49(2):566-573. doi: 10.3906/sag-1806-33. PubMed 30893985 ↗

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04389515
Lead sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Responsible party
Merve Aldikactioglu Talmac, MD (Specialist of Obstetrics and Gynecology, Principal Investigator, Kanuni Sultan Suleyman Training and Research Hospital) — Principal investigator
First posted
May 15, 2020
Start date
May 14, 2020
Primary completion
Sep 25, 2020 (estimated)
Completion
Sep 30, 2020 (estimated)
Last update
Sep 2, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion