Efficacy of a Nursing Intervention in First-time Mothers

February 2, 2020 updated by: Carolina Vargas Porras, University Rovira i Virgili

Efficacy of a Nursing Intervention in the Process of Becoming a Mother, in First-time Mothers

Experimental study will determine the efficacy of nursing intervention named Maternal support to become first-time mothers based on the theory of Ramona Mercer. Sequential explanatory design will be used. It is a mixed design with approach quantitative and qualitative in order to obtain a better approach of the phenomen. The approach quantitative will be randomized controlled clinical trial. The qualitative analysis of the content will be done according to Bardin.

Study Overview

Detailed Description

Taking into account the scientific literature related to studies in first-time mothers with healthy newborns, it can be concluded that the limited success of interventions that have been made suggests that the main areas of becoming a mother have not been addressed, either as part of the content or process of the interventions. This study will be conducted in 24 months. The sample size calculated will be 74 first-time mothers in total, which are allocated in two groups, intervention and control. Each group with 37 mothers.

Study Type

Interventional

Enrollment (Actual)

76

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Santander
      • Bucaramanga, Santander, Colombia, 680003
        • Clinica Materno Infantil San Luis

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 54 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Postpartum stage (for vaginal or for cesarean delivery)
  • Mother of a healthy full term newborn.
  • First-time mother.
  • Self-declared support by her couple.
  • Mother living in Bucaramanga metropolitan area

Exclusion Criteria:

  • Multiple pregnancy.
  • Mothers who cannot read or write.
  • Diagnosis of postpartum depression, mental disorders, behavioral disorders.
  • Mothers admitted to the intensive care unit after childbirth.
  • Mothers with newborns hospitalized in the intensive care unit, intermediate care or minimal care.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Maternal support to become mother

Maternal support to become mother: is an intervention based on the mid-range nursing theory of Ramona Mercer, whose purpose is to empower first-time mothers in their new maternal role, favoring the mother-child bond, strengthening social support and maternal self-efficacy, consists of:

  1. Four Home visits , in the first week; first month of baby life; at three months; and the fourth postpartum month.
  2. Four Educational sessions and support sessions for maternal empowerment in each home visit.
  3. Telephone follow-up: at 15 days; a month and a half; at two and a half months; and three and a half months postpartum.

"AMACOM-PRI": Apoyo Materno para Convertirse en Madre - Primerizas. Maternal support to become first-time mothers is an intervention based on the mid-range nursing theory of Ramona Mercer, whose purpose is to empower first-time mothers in their new maternal role, favoring the mother-child bond, strengthening social support and maternal self-efficacy, consists of.

  1. Four Home visits , in the first week; first month of baby life; at three months; and the fourth postpartum month.
  2. Four Educational sessions and support sessions for maternal empowerment in each home visit.
  3. Telephone follow-up: at 15 days; a month and a half; at two and a half months; and three and a half months postpartum.
Active Comparator: Control group: usual Care
The participants will receive the usual education about the care of the mother during the puerperium, the care of the newborn, including breastfeeding.

This intervention is usual care, which consists of:

  1. care of the mother and her newborn during the puerperium
  2. Teaching about breastfeeding.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scale name unabbreviated: "La escala de Adopción del Rol Materno (ARM) de la Doctora María del Carmen Garrido Hidalgo y la Doctora Marleny Marchán Coronado".
Time Frame: 4 Months
Construct: This scale measures the process of maternal role adoption or "becoming mother" process; such process and this scale was created based in Ramona Mercer's theory. Conformation: It consists of 56 items distributed in 10 dimensions: 1)Interaction with the couple with respect to the baby, 2)baby acceptance, 3 Contact with the role of mother, 4)Stimulation of the baby, 5)Interaction with the family of origin regarding to the baby, 6 Baby care, 7)Maternal expressions of affection for the baby, 8)Well-being of the baby, 9)Concern and protection of the baby, 10)Knowledge and culture related to the baby. Scale Scores and Ranges: The instrument has a Likert scale (from 1 to 4). 1 = totally disagree and 4 = total agreement. The score are from 56 to 224. The classification score ranges are: low 56-180 points, medium 181-202 and high 203-224 points. The higher score across the scale indicate better adoption of the maternal role. The outcome of this scale is the sum of each linker-item.
4 Months
Perceived Maternal Parenting Self-Efficacy (PMP S-E) by Dr. Christopher R. Barnes and Dr. Elvidina N. Adamson-Macedo: measures maternal self-efficacy.
Time Frame: 4 months
_this scale measures Perceived Maternal Parenting Self-Efficacy.Conformation: This instrument was created by two psychologists from the University of Wolverhampton, Ireland. It has validity and reliability studies in Ireland and Brazil. It consists of 20 items distributed in 4 dimensions_ 1. Care tasks, 2. Behaviors raised, 3. Reading of behaviors or signals, 4. Situational beliefs. Scale Scores and Ranges_ the instrument has a Likert scale that goes from 1 to 4. There are 1 in totally disagree and 4 in total agreement. The instrument has a minimum score of 20 and a maximum score of 80. The higher the scores indicate greater (better) self-efficacy_
4 months
"Perinatal Infant Care Social Support Scale" (PICSS) by Dr. Patricia Leahy-Warren: Construct: measures social support and has been widely applied in first-time mothers.
Time Frame: 4 months
Conformation: This instrument was created by a nurse from the University of College Cork, Ireland. It has validity and reliability tests in Ireland. Consisting of two subscales, the Structural Social Support subscale measures structural social support and the Functional Social Support subscale that measures functional social support. The latter is the one that is consistent with Ramona Mercer's nursing theory. The subscale Functional Social Support consists of 16 items distributed in 4 dimensions: 1) Informative Support, 2) Instrumental Support (Physical), 3) Emotional Support, 4)Valuation Support. Dimensions: Informative support (Minimum score of 7, maximum score of 28). Instrumental support (score range 7-28). Emotional support (score range 4- 16). Valuation support (score range from 4-16). The instrument has a Likert scale from 1 to 4; 1 for totally disagree and 4 for total agreement. Score range: 22-88. As higher the score, greater (better) Structural Social Support.
4 months
"Bond between parents and children of MSc Alix Nathalya Vargas Vásquez and Doctor Myriam Patricia Pardo Torres"
Time Frame: 4 months
_measures the affective bond between parents and children. This instrument was created by two nurses from the National University of Colombia, Colombia. It has validity and reliability tests in Colombia and Ecuador. Conformation_ Consists of 24 items distributed in 4 dimensions_ 1. Emotional support, 2. Union - interaction, 3. Informative support, 4. Stress. Score and ranges_ the instrument has a Likert scale that goes from 0 to 5. The instrument has a minimum score_ 24 and maximum score_ 96. The low degree of affective bonding is 85 points or less
4 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessing the experience of motherhood: The Being a Mother Scale (BaM-13) - Spanish adaptation (by Drs. Lucy Marcela Vesga Gualdrón and Maria Mercedes Durán de Villalobos)
Time Frame: 4 months
This instrument in its original English version was created by the psychologist Stephen Matthey and subsequently, based on this scale, with prior authorization, the nurses Dr. Vesga and Dr. Durán validated the Spanish scale. It is a self-report scale of 13 items. Cut point recommended is 9, which allows the classification of mothers according to the score obtained: greater than 9 is a risk of stress due to the maternal role and less than 9 is without risk of stress due to the maternal role.
4 months
Edinburgh Postnatal Depression Scale (EPDS) of Doctors J.L. Cox; JM Holden and R. Sagovsky (Spanish)
Time Frame: 4 months
Construct: measures postpartum depression. This instrument was created by three doctors from the University of Keele, United Kingdom. It has been widely used in several countries and has validity and reliability tests also in Colombia. It is made up of items 10. The categories of the answers are given points of 0, 1, 2 and 3 according to the increase in the severity of the symptom. The points for questions 3, 5, 6, 7, 8, 9, 10 are noted in reverse order (for example, 3, 2, 1, 0). All points are added to give the total score. Score and range: Score range from 0 to 10. A score of 10+ shows the probability of a depression, but not its severity. Any number that is chosen other than "0" for question number 10, means that it is necessary to do additional evaluations immediately. The EPDS score is designed to assist clinical judgment, do not replace the complete clinical evaluation.
4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 2, 2018

Primary Completion (Actual)

September 20, 2019

Study Completion (Actual)

February 1, 2020

Study Registration Dates

First Submitted

July 6, 2018

First Submitted That Met QC Criteria

July 18, 2018

First Posted (Actual)

July 20, 2018

Study Record Updates

Last Update Posted (Actual)

February 5, 2020

Last Update Submitted That Met QC Criteria

February 2, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 0418

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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