The Correlation Between Maternal Infant Bonding, Pain and Postpartum Depression

Sponsor
Rabin Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05206552
Collaborator
(none)
200
1
17.9
11.1

Study Details

Study Description

Brief Summary

The delivery process can be associated with significant maternal pain. which has many long and short term affects.

The aim of our study is to assess whether pain during and after childbirth negatively impacts a mother's attachment to her baby (maternal bonding) and the increases the incidence of postpartum depression.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire

Detailed Description

Delivery is a process that is correlated with maternal pain. The maternal pain can have signifcant long term and short term maternal and neontal impact.

The most common method for pain reilef during delivery is epidural analgesia. Few studies have examined the assocaition between use of epidural analgesia and postpartum depression, with some studies showing a postive correlation and other condricting so.

Maternal bonding is defined as her's emotional state, including maternal feelings towards the infant, it has proven to be the basis for the child's later attachment and sense of self.

A stable and strong bond between mother and child is associated with positive parental behavior and of the child's cognitive and behavioral development, while a unstable maternal infant bond can may lead to long term matenal and infant complications.

The aim of our study is to assess whether pain during and after childbirth negatively impacts a mother's attachment to her baby (maternal bonding) and the increases the incidence of postpartum depression.

In this study women the day after labor will be approched , following obtaining consent will be requested to fill out a the PBO vailadited maternal bonding questtionanire , the valadited EPDS (endinbough postpartum depression questionnaire) and a general questionnaire detailing their demographic , obstetric history and pain levels.

At six weeks postpartum a member of the research team will call the study participant and ask the PBO and EPDS questionnaires to asses the correlation between delivery pain , maternal bonding and postpartum depression,

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Correlation Between Maternal Infant Bonding , Pain and Postpartum Depression a Prospective Observational Cohort Study
Anticipated Study Start Date :
Jan 25, 2022
Anticipated Primary Completion Date :
Jan 25, 2023
Anticipated Study Completion Date :
Jul 25, 2023

Arms and Interventions

Arm Intervention/Treatment
Parturients above the age of 18

Study participants will include women after labour whom gave birth to a healthy neonate at 37 weeks with the ability to comply with study requirments

Other: Questionnaire
Maternal - Infant bonding questionnaire. EPDS - Postpartum depression questionnaire

Outcome Measures

Primary Outcome Measures

  1. Pain verbal numerical score after labor and maternal infant bonding. [24 hours after labor]

    pain levels graded from one to ten will be correlated with maternal infant bonding

Secondary Outcome Measures

  1. Pain verbal numerical score after labor and postpartum depression [6 weeks after labor]

    pain levels graded from one to ten will be correlated with postpartum depression defined as a score of above 10 on the edinbough postpartum depression score questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Months and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Women whom have givrn birth at rabin medical center with the ability to follow study requirments

Exclusion Criteria:

Women given birth to twins Women whos baby was hospitilzed Women who were treated with magnizum Women whos babies were born with congenital malformations

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beilinson hospital Petach tikvah Israel

Sponsors and Collaborators

  • Rabin Medical Center

Investigators

  • Principal Investigator: sharon orbach-zinger, Rabin Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
sharonorbach, prinicipal investigator, Rabin Medical Center
ClinicalTrials.gov Identifier:
NCT05206552
Other Study ID Numbers:
  • 0514-21
First Posted:
Jan 25, 2022
Last Update Posted:
Jan 25, 2022
Last Verified:
Jan 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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 25, 2022