Mediating Effects of Dyadic Coping on Parenting Stress and Parenting Self-efficacy in Parents of Preterm Infant

Sponsor
Sun Yat-sen University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05592210
Collaborator
(none)
308
1
15
20.6

Study Details

Study Description

Brief Summary

The goal of this observational study is to investigate the parenting stress, parenting self-efficacy and dyadic coping of preterm parents and explore the influence and pathway analysis of dyadic coping between parenting stress and parenting self-efficacy.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaires

Detailed Description

For now, there is a lack of investigation and research on parenting stress, parenting self-efficacy and dyadic coping of co-parenting for discharged premature infants in the literature, and the mediating effect of dyadic coping between parenting stress and parenting self-efficacy of preterm parents has not been verified yet. This study aims to provide a theoretical basis for effective intervention for preterm parents with high parenting pressure and insufficient parenting self-efficacy in clinical work.

Study Design

Study Type:
Observational
Anticipated Enrollment :
308 participants
Observational Model:
Case-Only
Time Perspective:
Other
Official Title:
Mediating Effects of Dyadic Coping on Parenting Stress and Parenting Self-efficacy in Parents of Preterm Infant
Anticipated Study Start Date :
Dec 1, 2022
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Questionnaires assessed Parents of preterm infants

Inclusion criteria for parents Parents of hospitalized preterm infants with a gestational age of less than 37 weeks; Both parents are at least 18 years old; Able to read and communicate in Chinese, able to complete the questionnaire independently or with the help of the investigator; Inclusion criteria for infant Gestational age less than 37 weeks; admitted to the NU or NICU and discharged after treatment;

Other: Questionnaires
Participants will be asked to fill out the the Demographic Information Sheet, Tool to Measure Parenting Self-efficacy, Parenting stress Index-short From and Dyadic Coping Inventory.

Outcome Measures

Primary Outcome Measures

  1. Tool to Measure Parenting Self-efficacy [baseline]

    The Parenting Self-efficacy of preterm parents will be measured by Tool to Measure Parenting Self-efficacy. The scale adopts Likert11-level scoring method, with 0 representing completely disagree and 10 representing completely agree. The higher the scores of each dimension and the total score, the higher the self-efficacy of the Parenting Self-efficacy of preterm parents.

  2. Parenting Stress Index-short From [baseline]

    The Parenting Stress of preterm parents will be measured by Parenting Stress Index-short From. The scale was scored from 1(strongly disagree) to 5(strongly agree) points, and the higher the score, the higher the feeling of parenting stress.

  3. Dyadic Coping Inventory [baseline]

    The Dyadic Coping of preterm parents will be measured by Dyadic Coping Inventory. The total score ranges from 36 to 180.. The higher the score, the more supportive behaviors the partner gives.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion criteria for parents

  • Parents of hospitalized preterm infants with a gestational age of less than 37 weeks;

  • Both parents are at least 18 years old;

  • Able to read and communicate in Chinese, able to complete the questionnaire independently or with the help of the investigator;

Inclusion criteria for Infants

  • Gestational age less than 37 weeks;

  • admitted to the NU or NICU and discharged after treatment

Exclusion criteria for parents

  • Single-parent family;

  • Parents diagnosed with severe anxiety and depression;

Exclusion criteria for Infants

  • for birth defects cannot be cured and affect the quality of life;

  • infants who were given up treatment due to illness or family reasons;

  • transferred or death;

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sun Yat-sen University Guangzhou China

Sponsors and Collaborators

  • Sun Yat-sen University

Investigators

  • Principal Investigator: Wei Xia, PhD, Sun Yat-sen University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wei XIA, PhD, Associate professor, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT05592210
Other Study ID Numbers:
  • preterm infant(PES)
First Posted:
Oct 24, 2022
Last Update Posted:
Oct 24, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wei XIA, PhD, Associate professor, Sun Yat-sen University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 24, 2022