Efficacy of Parent-child Sleep Intervention

Taipei Veterans General Hospital

Status: Completed

Conditions: Infant Health; Sleep Quality; Psychological Health

Treatments: Behavioral: parent-child sleep intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT06143917

2023-10-012C

Details and patient eligibility

About

Background: Parents of healthy neonates commonly face sleep disruptions and disturbances after delivery. Notably, increasing challenges are evident among parents of ill infants who required clinical care after birth . These challenges can adversely affect psychological adaptation and parental efficacy which consequently impacting the infant's development. It is crucial to develop an effective parent-child sleep intervention for improving parent-infant sleep and mental well-being and uneventful family health outcomes.

Aim: To develop and evaluate the effects of parent-child sleep intervention on improving sleep quality, psychological health, and infant health in parents of infants at intermediate care nursery.

Methods: A randomized controlled trial will be conducted at the intermediate care nursery of a level III medical center at Taipei city. A total of 102 pairs of parents and infants will be recruited and randomly assigned to the experimental group or the control group. The intervention program consists of (1) parent-child sleep education, (2) heart rate variability biofeedback training, and (3) counseling and support. Data collection will be multiple time points, including baseline, 1 month postpartum, 3 months postpartum, and 6 months postpartum.

Anticipated results: Developing and evaluating a parent-child sleep intervention for postpartum parents and their infants. The findings will be an empirical evidence for pediatric care and family health promotion.

Full description

The following measures will be used, including Insomnia Severity Index, Pittsburgh Sleep Quality Index, Brief Infant Sleep Questionnaire-Revised short form, Parental Efficacy Scale, State-Trait Anxiety Inventory, Infant Health Outcome Questionnaire. Objective data included actigraphy, and heart rate variability. Data will be analyzed using descriptive statistics and One-Way repeated measure ANOVA to examine the effectiveness of the intervention.

Enrollment: 306 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Postpartum women aged 18 years or older.
• Postpartum women with a singleton pregnancy, and the gestational age of their infant is at least 32 weeks.
• Postpartum women with a severe insomnia severity index score of ≥8 points.
• Postpartum women and their husbands or partners capable of reading, understanding, and communicating in Mandarin.
• Postpartum women and their husbands or partners with internet access and the ability to operate resources using a smartphone, tablet, or computer.
• Both postpartum women and their husbands or partners are willing to participate in the research process.

Exclusion criteria

• Postpartum women diagnosed with Insomnia Disorder, Anxiety Disorders, or Depression.
• Postpartum women suffering from arrhythmia or cardiovascular diseases.
• Postpartum women working in shifts.
• Infants with congenital abnormalities, neurological impairments (such as hydrocephalus, periventricular leukomalacia), requiring the use of tubes or respirators after discharge, or using medications that might affect sleep (such as caffeine, sedatives, muscle relaxant, anti-epileptic drugs, or pain medications).

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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306 participants in 2 patient groups

parent-child sleep intervention

Experimental group

Description:

Participants in the intervention will receive both the standardized usual care and parent-child sleep education, heart rate variability biofeedback training, and counseling and support.

Treatment:

Behavioral: parent-child sleep intervention

Control

No Intervention group

Description:

Participants in the control group will receive attention from the research nurse and the standardized usual care.