A Sustainable Choice to Reduce Carbon Footprint

December 16, 2025 updated by: Leyla Kaya, Saglik Bilimleri Universitesi

Breastfeeding: A Sustainable Choice to Reduce Carbon Footprint

This study aimed to evaluate the impact of carbon footprint education on breastfeeding practices among pregnant women.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study aimed to evaluate the impact of carbon footprint education on breastfeeding practices among pregnant women.

In the sample size calculation performed using G*Power 3.1.9.7 (Faul et al., 2007) software, the effect size value determined for the relationship between awareness levels regarding sustainable and healthy nutrition behaviors and reducing ecological footprint was determined as Cohen's r=0.470. Statistical power analysis was performed under A Priori: Compute required sample size (Correlation: Bivariate normal model), 95% power (1-β) and α=0.05 and in the light of these parameters, it was concluded that a sample size of at least 53 participants was required for the study in question. In case of data loss, it was envisaged to increase the sample by 20% as a result of statistical consultancy. Accordingly, it was planned to conduct the study with a total of n=64 people, n=32 in the intervention group and n=32 in the control group.

It was carried out with the participation of two groups. The carbon footprint education group received 4 education sessions of 60 minutes each. The control group received routine hospital care during this period, but no other intervention was made.

Data for the study were collected by the researcher using face-to-face interviews, a personal information form with demographic questions, and the measurement tools used in the study. The training was completed 4 weeks later. After the training, the measurement tools were used for the woman's postpartum period.

Participants were given an explanation of the carbon footprint education and told how, for how long, and where the education would take place. The carbon footprint education programme was completed by the participants in a specific way (nutrition, breastfeeding, environmental awareness) for each session. The education was delivered using a poster.

The carbon footprint education was given in 4 sessions in this way. The measurement tools were given to the participants again on the 1st day, 1st month, 3rd month and 6th month after birth.

Study Type

Interventional

Enrollment (Actual)

100

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 Locations

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Pregnant women 24 weeks gestation
  • Must be between 18 and 35 years of age.
  • Women must provide informed consent to participate in the study, indicating their willingness to participate in the educational intervention and assessments.
  • Attend educational sessions

Exclusion Criteria:

  • Women with significant medical conditions that may affect breastfeeding or nutrition (e.g. serious mental illness, chronic disease) will be excluded.
  • Multiple pregnancies
  • Previous GREEN MOTHER training
  • Substance abuse
  • Women considered to be at high risk of non-compliance with the study protocol (e.g. those with unstable living conditions).

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Women in the control group receive routine care at the same hospital's polyclinics.
Experimental: Experimental

Women selected for the experimental group will receive 4 sessions of Green Mother Training.

The programme, which includes breastfeeding, bonding and carbon footprint training, is delivered 4 times by researchers.

The training content has been prepared by the researchers by scanning the literature. The training will be delivered using posters.

Poster education

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scale Breast-feeding Self-efficacy Scale
Time Frame: 1st day after birth, 3rd month after birth, 6th month after birth
Breastfeeding Self-Efficacy Scale: This is a 33-item scale developed by Dennis (1999). It consists of two sub-dimensions to determine mothers' breastfeeding skills, beliefs and behaviours regarding breastfeeding. The validity and reliability study of the Turkish form of the scale was conducted by Ekşioğlu and Çeber (2011). Breastfeeding self-efficacy was assessed using a five-point Likert scale: (1) I never trust myself, (2) I do not trust myself very much, (3) I trust myself sometimes, (4) I trust myself often, (5) I always trust myself. As the total score on the scale increases, so does breastfeeding self-efficacy. The lowest score is 33 and the highest is 165.
1st day after birth, 3rd month after birth, 6th month after birth
Ecological Footprint Awareness Scale
Time Frame: Participants immediately after group assignment, 6 months after the birth
The Ecological Footprint Awareness Scale consists of six sub-dimensions: energy, legal, recycling, transport, water use and food. The scale categories are obtained by summing the subscales and scoring them as strongly disagree=1, disagree=2, undecided=3, agree=4 and strongly agree=5. The Cronbach's alpha value was found to be 0.960.
Participants immediately after group assignment, 6 months after the birth
Behaviors Scale Towards Sustainable Nutrition
Time Frame: Participants immediately after group assignment, 6 months after the birth
The developed scale consists of 29 items and 4 sub-dimensions with a five-point Likert scale. It includes the sub-dimensions of food preference, reducing food waste, eating seasonally and locally, and buying food. The scale is rated as 'never', 'rarely', 'sometimes', 'often' and 'always'. All items are scored from 1 to 5, starting with 'never'. All items in the scale are positive. The lowest score that can be obtained from the scale is 29 and the highest score is 145. Sub-dimension scores are obtained by dividing the sum of the scores given by individuals to the questions in the sub-dimension by the number of questions in the sub-dimension. Higher total and sub-dimension scores indicate that the individual has more sustainable dietary behaviours.
Participants immediately after group assignment, 6 months after the birth
Depression Anxiety and Stress scales-21 (DASS-21)
Time Frame: Participants immediately after group assignment, 1st day after delivery, 3rd month after delivery, 6th month after delivery
his 21-item scale consists of three dimensions, namely anxiety, depression, and stress. Items are measured on a 4-point Likert-type scale ranging from 0 (Never) to 3 (Always). A higher sum score indicates more severe symptoms of depression, anxiety, and stress.
Participants immediately after group assignment, 1st day after delivery, 3rd month after delivery, 6th month after delivery

Collaborators and Investigators

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

Investigators

  • Study Director: Esra Keles, PhD, Saglik Bilimleri Universitesi

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)

January 31, 2025

Primary Completion (Actual)

August 6, 2025

Study Completion (Actual)

December 16, 2025

Study Registration Dates

First Submitted

January 13, 2025

First Submitted That Met QC Criteria

January 13, 2025

First Posted (Actual)

January 17, 2025

Study Record Updates

Last Update Posted (Actual)

December 23, 2025

Last Update Submitted That Met QC Criteria

December 16, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 06.09.2023/118

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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