- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05206552
The Correlation Between Maternal Infant Bonding, Pain and Postpartum Depression
The Correlation Between Maternal Infant Bonding , Pain and Postpartum Depression a Prospective Observational Cohort Study
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.
Study Overview
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 Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Petach tikvah, Israel
- Recruiting
- Beilinson Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
*Women whom have given birth at rabin medical center with the ability to follow study requirements.
Exclusion Criteria:
- Women given birth to twins
- Women who's baby was hospitalized
- Women who were treated with magnesium
- Women who's babies were born with congenital malformations
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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
|
Maternal - Infant bonding questionnaire.
EPDS - Postpartum depression questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain verbal numerical score after labor and maternal infant bonding.
Time Frame: 24 hours after labor
|
pain levels graded from one to ten will be correlated with maternal infant bonding
|
24 hours after labor
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain verbal numerical score after labor and postpartum depression
Time Frame: 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
|
6 weeks after labor
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0514-21
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Maternal Care Patterns
-
Assiut UniversityNot yet recruitingMaternal Care Patterns
-
Halic UniversityCompletedMaternal Behavior | Maternal Care PatternsTurkey
-
Necmettin Erbakan UniversityNot yet recruitingSelf Efficacy | Maternal Behavior | Maternal Care PatternsTurkey
-
JhpiegoBill and Melinda Gates Foundation; Addis Continental Institute of Public Health and other collaboratorsCompletedMaternal Care PatternsEthiopia, Kenya, Nigeria
-
Assiut UniversityCompletedMaternal Care PatternsEgypt
-
World BankUnknownMaternal Care Patterns
-
Dilla UniversityEthiopian Public Health Institute; Ministry of Health, EthiopiaCompleted
-
University of California, DavisHealth Resources and Services Administration (HRSA)CompletedPregnancy Related | Breastfeeding | Maternal Care PatternsUnited States
-
Hirabai Cowasji Jehangir Medical Research InstituteActive, not recruitingMaternal Health | Feeding Patterns | Prenatal CareIndia
-
Oregon Health and Science UniversityUniversidad de AntioquiaCompletedPregnancy Related | Contraception | Maternal Care PatternsColombia
Clinical Trials on Questionnaire
-
H. Lee Moffitt Cancer Center and Research InstituteSan Diego State University; University of Minnesota; University of ArizonaCompletedAnxiety | Psychological StressUnited States
-
Centre Hospitalier Universitaire de NiceCompletedGeneral Population | TDAH | Children Aged 5 to 18 YearsFrance
-
Stanford UniversityRecruitingAstigmatism | Nearsightedness | FarsightednessUnited States
-
University Medical Center GoettingenCompletedOrofacial Pain | Sleep ProblemsGermany
-
University of LiegeCompletedCritical Illness | Covid19 | Psychological Stress | FamilyBelgium
-
Imperial College Healthcare NHS TrustNot yet recruitingCervical Myelopathy
-
Children's Hospitals and Clinics of MinnesotaCompletedFirearm Injury | Firearm Safety | Firearm OwnershipUnited States
-
Fondazione Policlinico Universitario Agostino Gemelli...Recruiting
-
Imperial College LondonRoyal Marsden NHS Foundation Trust; University College London Hospitals; The... and other collaboratorsCompleted
-
University Hospital, Clermont-FerrandCompletedQuality of Life | Dentin HypersensitivityFrance