ClinicalTrials.gg
RecruitingNCT07890142Updated Oct 22, 2026

Experiences of Mothers Considering Breastfeeding Cessation: Decision-Making, Method Exploration, and Support Needs

An observational study in Breastfeeding Cessation, sponsored by Istanbul University - Cerrahpasa. Recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Istanbul University - Cerrahpasa · Observational

Updated Oct 22, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
25
Ages
18 Years and older
Sex
Female
01

Study summary

This study aims to explore the experiences of mothers who are currently breastfeeding their children but are considering stopping breastfeeding. It focuses on how mothers make decisions about breastfeeding cessation, where they seek information about possible methods, what uncertainties or difficulties they experience, and what support they need from healthcare professionals.

This is a qualitative study using a phenomenological approach. Approximately 20 to 25 mothers aged 18 years or older who are currently breastfeeding a child aged at least 6 months and are considering breastfeeding cessation will be invited to participate. The final number of participants will depend on the information obtained during the interviews.

Data will be collected through individual, semi-structured interviews lasting approximately 30 to 45 minutes. Participants will also complete a brief form about their demographic characteristics and breastfeeding experiences. Interviews will be conducted face-to-face or online, depending on participant preference.

The findings are expected to provide a better understanding of mothers' experiences and support needs during the breastfeeding cessation decision-making process and may help inform breastfeeding counseling provided by healthcare professionals.

Read the detailed description

The study uses a qualitative phenomenological design and does not follow a cohort, case-control, or other conventional epidemiological observational study model. This qualitative study will use a phenomenological approach to explore the experiences of mothers who are currently breastfeeding and considering breastfeeding cessation. The study seeks to gain an in-depth understanding of mothers' decision-making processes, their exploration of breastfeeding cessation methods and information sources, the uncertainties and difficulties they experience or anticipate, and their perceived support needs.

Participants will be recruited using purposive sampling, with an emphasis on maximum variation to capture diverse experiences and stages of decision-making. Recruitment will take place through social media platforms, mother-child groups, and relevant online communication channels. Snowball sampling may also be used. Approximately 20 to 25 mothers are expected to participate, although the final sample size will be determined based on data saturation.

Data will be collected using a 17-item Participant Information Form and an eight-question Semi-Structured Interview Guide developed by the researchers based on the relevant literature. Individual interviews will be conducted face-to-face or online according to participant preference and are expected to last approximately 30 to 45 minutes. With participants' permission, interviews will be audio-recorded and transcribed verbatim.

Descriptive data will be summarized using appropriate descriptive statistics. Qualitative interview data will be analyzed using thematic analysis. Interview transcripts will be read repeatedly to achieve familiarity with the data, followed by initial coding, development of candidate themes and subthemes, review and refinement of themes, and definition and reporting of the final themes. MAXQDA 24 software will be used to support the organization and analysis of qualitative data. Data collection and analysis will be conducted concurrently, and data collection will end when additional interviews no longer provide meaningful new information, codes, or themes relevant to the research questions.

The study does not involve an investigator-assigned intervention. Its purpose is to understand mothers' experiences and perceived support needs rather than to evaluate the effectiveness of breastfeeding cessation methods.

02

Conditions studied

  • Breastfeeding Cessation

Keywords

  • Breastfeeding Cessation
  • Weaning
  • Maternal Experiences
  • Decision-Making
  • Support Needs
  • Qualitative Research
03

In context

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 693 studies on the registry; 213 are open to participants now.

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

04

Who can participate

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

Study population

The study population will consist of mothers aged 18 years or older who are currently breastfeeding a child aged at least 6 months and are considering breastfeeding cessation. Participants will be recruited through social media platforms, mother-child groups, and relevant online communication channels. Purposive sampling will be used to include mothers with diverse experiences and at different stages of decision-making regarding breastfeeding cessation. Snowball sampling may also be used.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18 years or older.
  • Having given birth at least once.
  • Currently breastfeeding their child.
  • Having a child aged at least 6 months.
  • Actively considering or planning breastfeeding cessation.
  • Being in the process of making decisions about breastfeeding cessation and/or determining cessation methods.
  • Being able to communicate in Turkish.
  • Voluntarily agreeing to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Having completely stopped breastfeeding.
  • Not considering breastfeeding cessation.
  • Having communication difficulties that prevent participation in the interview.
  • Having any condition that prevents completion of the research interview.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
25 participants (estimated)
Patient registry
No

Groups and cohorts

  • Mothers Considering Breastfeeding Cessation

    Mothers aged 18 years or older who are currently breastfeeding a child aged at least 6 months and are actively considering or planning breastfeeding cessation. Participants will be recruited using purposive sampling, with an emphasis on maximum variation. Data will be collected through individual semi-structured interviews. No intervention will be assigned by the researchers. Kopyala

06

What researchers measure

Primary outcomes

  1. Experiences of Mothers Considering Breastfeeding Cessation

    Mothers' experiences regarding breastfeeding cessation will be explored through individual semi-structured interviews. The interviews will examine decision-making processes, information sources, exploration of cessation methods, uncertainties, anticipated or experienced difficulties, and perceived support needs. Interview transcripts will be analyzed using thematic analysis to identify themes and subthemes reflecting participants' experiences.

    Time frame: During a single semi-structured interview (approximately 30-45 minutes) Kopyala

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07890142
Responsible party
Eslem Altıntaş (M.Sc., Acibadem University) — Principal investigator
First posted
Oct 22, 2026
Start date
Nov 2026 (estimated)
Primary completion
Mar 2027 (estimated)
Completion
Mar 2027 (estimated)
Last update
Oct 22, 2026

Study contacts

Eslem ALTINTAŞ, M.Sc.
Contact
kuruleslem@gmail.com
+90 541 610 54 12
Merve Coşkun, Ph.D.
principal investigator · Acibadem University
Güzin Ünlü Suvari, M.Sc.
principal investigator · Acibadem University

Oversight

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

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