Breastfeeding RatesNCT07913438
Development and Implementation of a Breastfeeding Program for Post-Cesarean Section Women Based on the 5A Nursing Model
A study testing Based on the 5A nursing intervention plan and Implement routine care in people with Breastfeeding Rates, run by The Third Xiangya Hospital of Central South University at 1 site in China.
Trial summary
Develop and apply a breastfeeding program for postoperative mothers of cesarean section based on the 5A nursing model, and evaluate its impact on the mothers' mastery of breastfeeding knowledge, self-efficacy, breastfeeding rate, and psychological state. Read more about this study
- Who is it for?
- Ages 18 to 50 years, women only
- Conditions the study is for
- Breastfeeding Rates
- What is being tested?
- Based on the 5A nursing intervention plan and Implement routine care
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteChina
- Study dates
- 11 Mar 2026to 11 Mar 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Normal mental state, capable of cooperating to complete the experiment;
- Full-term singleton pregnancy;
- Parturient who underwent cesarean section delivery.
Who cannot join
- Emergency cesarean section was performed during vaginal delivery;
- The pregnant woman had severe pregnancy complications or infectious diseases and was unable to breastfeed;
- The newborn was transferred to the neonatal department due to illness treatment;
- The mother strongly refused breastfeeding of her own will.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Develop and apply a breastfeeding program for postoperative mothers of cesarean section based on the 5A nursing model, and evaluate its impact on the mothers' mastery of breastfeeding knowledge, self-efficacy, breastfeeding rate, and psychological state.
- Conditions
- Breastfeeding Rates
- Being tested
- Based on the 5A nursing intervention plan, Implement routine care
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Based on the 5A nursing intervention planBehavioural
Based on literature research and qualitative interviews, and through the Delphi expert consultation method, a set of intervention measures was ultimately formulated.
Implement routine careBehavioural
Implement routine care
| Study group | Role | What they receive |
|---|---|---|
| Usual Care group | Active comparator | Implement routine care Receives: Behavioral: Implement routine care |
| Intervention group | Experimental | Not described Receives: Behavioral: Based on the 5A nursing intervention plan |
What is being measured
The primary outcome is the main question the study is designed to answer.
Exclusive breastfeeding rate
Measured: Three days after giving birth and 42 days after giving birth
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Nov 2026
- Study start11 Mar 2026
- Primary completion11 Mar 2027 (estimated)
- Study completion11 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breastfeeding RatesStudies of the same condition, open and under way.
- More trials run by The Third Xiangya Hospital of Central South UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07913438
- Sponsor's protocol ID
- E202626
- Status last verified
- Nov 2026
- First submitted
- 24 Aug 2026
- Last updated
- 3 Nov 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development and Implementation of a Breastfeeding Program for Post-Cesarean Section Women Based on the 5A Nursing Model
- ClinicalTrials.gov ID
- NCT07913438
- Acronym / sponsor ID
- E202626
- Conditions
- Breastfeeding Rates
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- The Third Xiangya Hospital of Central South UniversityUniversity, hospital or other
- Study start
- 11 Mar 2026 (actual)
- Primary completion
- 11 Mar 2027 (estimated)
- Study completion
- 11 Mar 2027 (estimated)
- First posted
- 3 Nov 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Develop and apply a breastfeeding program for postoperative mothers of cesarean section based on the 5A nursing model, and evaluate its impact on the mothers' mastery of breastfeeding knowledge, self-efficacy, breastfeeding rate, and psychological state.
Study design
- Primary purpose
- Supportive care
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Usual Care group | Active comparator | Behavioral: Implement routine careImplement routine care |
| Intervention group | Experimental | Behavioral: Based on the 5A nursing intervention plan |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Normal mental state, capable of cooperating to complete the experiment;
- Full-term singleton pregnancy;
- Parturient who underwent cesarean section delivery.
Key exclusion criteria (4 listed)
- Emergency cesarean section was performed during vaginal delivery;
- The pregnant woman had severe pregnancy complications or infectious diseases and was unable to breastfeed;
- The newborn was transferred to the neonatal department due to illness treatment;
- The mother strongly refused breastfeeding of her own will.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Based on the 5A nursing intervention planBased on literature research and qualitative interviews, and through the Delphi expert consultation method, a set of intervention measures was ultimately formulated. | Behavioural | Intervention group |
| Implement routine careImplement routine care | Behavioural | Usual Care group |
Primary outcome
Exclusive breastfeeding rate
Time frame: Three days after giving birth and 42 days after giving birth
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Nov 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Based on the 5A nursing intervention plan and Implement routine care in people with Breastfeeding Rates, run by The Third Xiangya Hospital of Central South University at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 3 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Exclusive breastfeeding rate (time frame: Three days after giving birth and 42 days after giving birth). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Nov 2026.