The Effectiveness of Audiovisual Intervention
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
AgeNot listed
SponsorChang Gung Memorial Hospital
About this trial
The objective of this clinical study is to understand the current status of parent-child bond, parenting role perception and well-being of fathers of preterm infants, and to explore the effect of audio-visual interventions on parent-child bonding, parenting role perception and well-being of fathers of preterm infants. The main questions it aims to answer are:
* After intervention, whether the parent-child connection between fathers and preterm infants in the audio-visual group is higher than that in the audio-visual group and the control group * After the intervention, whether the father's perception of parenting role in the audio-visual group is higher than that of the vocal group and the control group * After intervention, whether the father's happiness in the audio-visual group is higher than that in the audio-visual group and the control group The investigators will compare the pre- and post-test methods bwtween the experimental groups and the control group. The fathers of enrolled preterm infants will fill in the structured questionnaires at the time before the intervention (Baseline data) and one month later after the intervention.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
father age > 20
premature infant born at 29-36 weeks
Disqualifiers
infant failing the hearing examination
father and mother are not married
Trial design
Design model
Parallel
Treatments tested in this trial
Audiovisual Intervention
Behavioral【Group 1】During the first three days, the researchers will provide a storybook to the father of the premature infant, and the researchers assist in recording the father's voice of the storybook in the form of MP4 recording. At the fourth day, one hour after the baby feeding, the father's voice will be played by the player to the baby, for 2 consecutive days, 2 times/day, 10 minutes/time. The baby's heartbeat, breathing and blood oxygen changes will be recorded and monitored with a physiological monitor. The recording files will be kept by the researcher. 【Group 2】 The intervention will be the same with Group 1 except the following intervention: on the 4th-6th day of the baby's birth, sleeping in the incubator, the baby's reaction behavior will be taken with a mobile phone, 1 time/day, 5 minutes/time, for 3 consecutive days, the image feedback is delivered to the father in person.
Treatment groups
99 Participants
are divided into 2 treatment groupsGroup A: The Effectiveness of Audiovisual InterventionExperimental treatment 1 intervention
Group B: controlPlacebo comparator 1 intervention
Trial outcomes
Primary outcomes
1
Postpartum Bonding Questionnaire
This questionnaire was designed by Brockington et al and published in 2001. The scale is a 5-point Likert's score. The higher score means a better parent-child bounding.
Time frame
one month2
Paternal Role Significance Questionnaire
This questionnaire was designed by Bruce et al and published in 1999. The scale is a 4-point Likert's score. The higher score means a better significance of paternal role.
Time frame
one month3
Satisfaction With Life Scale
This questionnaire was designed by Diener et al and published in 1985. The scale is a 7-point Likert's score. The higher score means a better satisfaction with life.
Time frame
one month4
Positive and Negative Affect Schedule (PANAS)
This questionnaire was designed by Diener et al and published in 1995. The scale is a 7-point Likert's score. The higher score means more perceived happiness in life.
Time frame
one monthLocations
Sponsors and contacts
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Source ClinicalTrials.gov
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