The Effect of an Emancipatory Knowing-Based Training Program on the Carbon Footprint of Postpartum Nursing Care

March 10, 2026 updated by: HATİCENUR BALABAN KAPTAN, Ondokuz Mayıs University

The Effect of an Emancipatory Knowing-Based Training Program on the Carbon Footprint of Postpartum Nursing Care: A Quasi-Experimental Study

This study aims to examine the effect of a training program based on Emancipatory Knowing on nurses' awareness and practices related to carbon footprint reduction in postpartum nursing care. In the first phase of the study, the carbon footprint of postpartum nursing care procedures - including those performed after both vaginal and cesarean deliveries - will be measured and compared using a validated observation-based inventory. In the second phase, nurses working in postpartum units will receive a structured educational intervention developed within the PEACE+G model framework. Before and after the training, nurses' carbon footprint-related knowledge, attitudes, and behaviors will be assessed. Findings are expected to contribute to the development of environmentally sustainable nursing practices in women's health.

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Interventional

Enrollment (Estimated)

24

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

Study Contact Backup

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Working as a nurse in a postpartum unit Having at least 6 months of clinical experience in postpartum care Volunteering to participate in the study Being able to read and write in Turkish

Exclusion Criteria:

  • Being on leave (maternity, sick, or annual leave) during the study period Having previously received training on carbon footprint or environmental sustainability in healthcare Withdrawing consent to participate at any stage of the study

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

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Group
Nurses working in postpartum units who will receive a structured training program based on the PEACE+G model (Emancipatory Knowing framework) aimed at reducing the carbon footprint of postpartum nursing care.
The PEACE+G Training Program is a structured educational intervention developed based on the Emancipatory Knowing framework in nursing, extended with a Governance dimension. The program consists of theoretical and reflective practice sessions delivered to postpartum unit nurses. Content covers carbon footprint measurement in healthcare, environmentally sustainable postpartum nursing care practices, and nurses' roles in reducing greenhouse gas emissions. The training is organized around six core criteria: Praxis, Empowerment, Awareness, Cooperation, Evolvement, and Governance (PEACE+G). Pre-test and post-test assessments are conducted using the validated PEACE-KAİ instrument to evaluate changes in nurses' knowledge, attitudes, and behaviors regarding carbon footprint reduction in postpartum care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Carbon Footprint of Postpartum Nursing Care
Time Frame: Baseline (before intervention)
The carbon footprint (kg CO₂e) of postpartum nursing care procedures following vaginal and cesarean deliveries, measured using a validated observation-based carbon footprint inventory (PEACE-KAİ).
Baseline (before intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nurses' Carbon Footprint Knowledge, Attitude and Behavior
Time Frame: Baseline and immediately after intervention
Assessed using the validated PEACE-KAİ instrument before and after the PEACE+G training program.
Baseline and immediately after intervention
Comparison of Carbon Footprint Between Vaginal and Cesarean Delivery Postpartum Care
Time Frame: Baseline (before intervention)
Carbon footprint values (kg CO₂e) compared between two delivery types.
Baseline (before intervention)

Collaborators and Investigators

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

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 (Estimated)

April 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

June 1, 2027

Study Registration Dates

First Submitted

March 10, 2026

First Submitted That Met QC Criteria

March 10, 2026

First Posted (Actual)

March 16, 2026

Study Record Updates

Last Update Posted (Actual)

March 16, 2026

Last Update Submitted That Met QC Criteria

March 10, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2024-1283

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

19:54No individual participant data sharing is planned. The study involves healthcare professionals (nurses) as participants, not patients. Data will be reported only in aggregate form to protect participant confidentiality.

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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