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Sensitivity Training for Parents With Premature Infants

Sensitivity Training for Mothers With Premature Infants: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04383340
Enrollment
68
Registered
2020-05-12
Start date
2018-02-01
Completion date
2019-08-31
Last updated
2022-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature Birth

Keywords

sensitivity training, mother-infant interaction

Brief summary

This study evaluated the effectiveness of a culturally adapted version of the Mother-Infant Transaction Program (MITP) among Chinese mothers with premature infants in public hospitals in Hong Kong.

Detailed description

Potential participants at two public hospitals in Hong Kong were identified by ward nurses. Mother-infant dyads with infants born at 36 weeks or earlier were assessed for eligibility. Data collection was conducted after obtaining written consent from the mothers. Mother-infant dyads who met the inclusion criteria were randomly allocated to either the intervention or the treatment-as-usual control group. Each dyad was assessed at six time points, i.e., baseline, immediately after intervention/TAU, and when the infants were at the gestation-corrected ages of 3, 6, 9, and 12 months.

Interventions

BEHAVIORALMother-Infant Transaction Program

Parent sensitivity training for mothers of premature infants

BEHAVIORALTreatment as usual

Standard hospital care and parental support

Sponsors

Hospital Authority, Hong Kong
CollaboratorOTHER_GOV
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Masking description

All individual assessments were conducted by a clinical psychologist at the hospital who was blinded to the experimental condition of the participants.

Intervention model description

Randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Mothers with premature infants born at 36 weeks or earlier

Exclusion criteria

* insufficient spoken and written Chinese ability of the mother * mother under 18 years of age * triplets or higher multiples * infants with congenital abnormalities (e.g., metabolic disorder, chromosomal disorder)

Design outcomes

Primary

MeasureTime frameDescription
Infant's temperamentAt baseline prior to interventionInfant's soothability based on the Infant Behavior Questionnaire. A higher average score denotes higher soothability of the infant, and the highest possible score is 7.
Behavioral observation of mother-infant interactionsAt baseline prior to interventionMaternal sensitivity and quality of mother-infant interaction measured by coding a 5-min video of mother-infant interaction. The coded variables are rated on a 5-point scale, and higher scores indicate higher maternal sensitivity and better interaction quality.
Maternal postnatal depressionAt baseline prior to interventionMaternal depression measured by the Edinburgh Postnatal Depression Scale. Possible scores range from 0 to 30. Higher scores indicate higher levels of depression.
Parenting stressAt baseline prior to interventionParenting stress measured by the Parenting Stress Index-Short Form. Possible scores range from 36 to 180. Higher scores indicate higher levels of parenting stress.
Infant's weight gainAt infant's corrected age of 3 monthsInfant's weight gain from birth
Infant's developmental outcomesAt infant's corrected age of 3 monthsMeasured by the Cognitive Battery of the Merrill-Palmer-Revised Scales of Development, which includes assessments in the cognitive, receptive language, and fine motor domains. Higher scores denote better performance in the assessments

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026