Relationship Between the Severity of Sleep Deprivation in the First 48 Hours Postpartum, Breastfeeding Motivation, and Breastfeeding Success

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorAcibadem University

About this trial

The postpartum period is a critical time marked by significant physiological and psychosocial changes that can affect sleep, emotional well-being, and breastfeeding behaviors. Previous studies indicate that mode of delivery and sleep quality are closely associated with breastfeeding outcomes, with cesarean birth often linked to poorer sleep and lower breastfeeding success. Evidence also suggests that postpartum sleep disturbances are related to reduced breastfeeding self-efficacy, lower motivation, fatigue, depressive symptoms, and shorter breastfeeding duration.

However, the literature lacks studies that evaluate insomnia severity, breastfeeding motivation, and breastfeeding success simultaneously-particularly during the first 48 hours after birth. This analytical study aims to assess insomnia severity, breastfeeding motivation, and breastfeeding success (LATCH) within the first 48 postpartum hours and to examine the relationships among these variables. Findings are expected to support early postpartum clinical interventions to improve maternal and infant health outcomes.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Primiparous or multiparous women aged 18 years and older

Having a healthy term delivery

Infant not admitted to the neonatal intensive care unit (NICU)

Initiated breastfeeding within the first 48 hours postpartum

Disqualifiers

Complications requiring sedation

Severe postpartum hemorrhage

Severe postoperative pain or need for narcotic analgesics

Trial population

The study population will consist of primiparous and multiparous women aged ≥18 years who have delivered a healthy term infant, whose newborn is not admitted to the NICU, and who initiated breastfeeding within the first 48 hours postpartum.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Breastfeeding Success (LATCH Score)

Breastfeeding success will be assessed using the LATCH Breastfeeding Assessment Tool, which evaluates five domains: latch, audible swallowing, type of nipple, maternal comfort (breast/nipple), and holding/positioning. Each item is scored from 0 to 2, with a total score ranging from 0 to 10. Higher scores indicate greater breastfeeding success.

Time frame
Within the first 48 hours postpartum (one-time assessment at enrollment)
2

Insomnia Severity (Insomnia Severity Index, ISI)

Insomnia severity will be measured using the Insomnia Severity Index (ISI), a 7-item self-report questionnaire assessing difficulty initiating sleep, difficulty maintaining sleep, early morning awakening, satisfaction with sleep, interference with daytime functioning, noticeability of impairment, and distress caused by sleep problems. Each item is scored from 0 to 4, yielding a total score of 0-28. Higher scores indicate more severe insomnia.

Time frame
Within the first 48 hours postpartum (one-time assessment at enrollment)
3

Breastfeeding Motivation (Breastfeeding Motivation Scale Subscale Scores)

Breastfeeding motivation will be evaluated using the Breastfeeding Motivation Scale based on Self-Determination Theory. The scale includes 24 items rated on a 4-point Likert scale and provides scores for five subdomains: integrated regulation, intrinsic motivation/identified regulation, introjected regulation (social approval), introjected regulation (social pressure), and external regulation (secondary benefits). Subscale scores are calculated as the mean of items within each subdomain; higher scores indicate stronger motivation of that type.

Time frame
Within the first 48 hours postpartum (one-time assessment at enrollment)
4

Maternal and Neonatal Characteristics (Descriptive Data Form)

Participant demographic, obstetric, delivery-related, neonatal, breastfeeding history, breastfeeding-related characteristics, and sleep habit information will be collected using a structured descriptive information form developed by the researchers based on the literature.

Time frame
Within the first 48 hours postpartum (one-time assessment at enrollment)

Secondary outcomes

Other outcomes

Sponsors and contacts

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