This quasi-experimental study is an educational support intervention protocol for infant care which will be conducted in two phases. The educational support program will be designed in the first phase. This program will be designed based on the review of previous studies and considering the opinions of the panel of experts in health education and promotion, pediatric nursing, and mother-infant health. The program includes educational sessions on breastfeeding, growth and development of infants and care for children under two years of age in a virtual group where a physician, a nurse, a midwife and a healthcare provider are also present. Using the opinions of the experts, the peer group will discuss various points and the research team will finalize the program based on priorities. Reminder text messages will be sent to the participants to remind them of the educational program. The second phase of the educational intervention will be conducted experimentally as a pretest-posttest design for the intervention and control groups.
Aim
This study seeks to design and implement an educational support program for infant care through sharing the experiences of peers, which will be able to affect the indicators of infant growth, breastfeeding self-efficacy and quality of life of mothers.
Research hypotheses
Given the main objective of the study, a hypothesis will be considered based on the opinions of health education, pediatric nursing and mother-infant health experts. The hypothesis is that, after the intervention, the mean score of the indicators of infant growth, breastfeeding self-efficacy and quality of life of mothers will be more in the intervention group.
Phase I: Designing an Educational-Supportive Program
The design of the intervention and the identification of the target audience in this phase will be based on the review of the texts and similar studies as well as the opinions of experts. The educational support program will include virtual training sessions on breastfeeding, growth and development of infants and care for children under two years of age in a WhatsApp group where a physician, a nurse, a midwife and a healthcare provider are among the members. Moreover, the experiences of the peers will be used through discussions and exchange of information.
Virtual educational support sessions
All mothers of the intervention group will join the WhatsApp group, which is managed by the researchers. Additionally, other members of the virtual group include a midwife, a nurse, a healthcare provider and a family physician for answering the specialized questions of the mothers. Accordingly, with regard to their questions, the mothers will have access to nurse, physician and midwife.
In this group, two days a week, an educational program will be provided by the researcher in the form of educational packages related to breastfeeding, growth and development, vaccination, health and nutrition and other cares for children under two years of age for two months. The educational content has been shown in Table 1. These packages will be sent to mothers based on the latest references of pediatric nursing books approved by the Ministry of Health and the family physician. Two days after sending the educational materials to the mothers, the researcher (pediatric nurse) will provide the mothers with additional explanations about the educational content for 40 minutes and the mothers will ask their questions. The control group will use the routine services of health centers and, after the implementation of the program, the educational packages will be provided to them in the form of booklets.
Peer group experiences
In addition to virtual sessions, the mothers of this group will be able to share their experiences with regard to the growth and development of their infants in this space for a period of three months. At the beginning of the study, the mothers will be informed that the prescription of chemical, herbal, and traditional medicines is against the rules of the research plan and in case of violating these rules, they will be removed from the group. Sharing the experiences of mothers with each other is limited to the issues of growth and development of a healthy child. The researcher and family physician will control all the messages of the intervention group members and prevent the mothers from confusion by providing them with correct guidance. Moreover, in case of illness and any clinical problems for the infant, it is recommended that mothers see a specialist in person.
Follow-up and sustained education
For follow-up and sustained education, reminders and encouragement messages will be sent to mothers at the end of each week. Additionally, to ensure the awareness and learning of research subjects at the end of the month, the mothers are assessed by answering questions extracted from the educational content taught by the researcher.
Table 1
Educational program
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Educational content
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How to provide education
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Audience
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Educational package
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Newborn
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Breastfeeding methods (time and duration of breastfeeding); milking and storing breast milk; KMC; bathing the infant; vaccination and aftercare; umbilical cord care; change of clothes; burping; methods of preventing sudden infant death syndrome; how to use supplements; Thyroid check-up (hypothyroidism training); education of danger and safety symptoms and the need for seeing a physician; and audiometry
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Educational program will be offered two days a week and for two months in the form of educational package which will be sent to the virtual group
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Mothers of infants
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One month to two years old
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Optometry; complementary nutrition; toilet training; infant safety; food allergies; vaccinations and aftercare; weaning education; oral health of the infant; development of social skills as well as delicate and coarse movements
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Question and answer
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Questions about the educational content and problems of the mothers and the response of the experts to these questions in the group
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Necessary additional explanations with regard to the educational content and questions asked by the mothers in the virtual group
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Mothers of infants
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Peer experiences
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Sharing the experiences of mothers with regard to the growth and development of their infants in a virtual group and under the supervision of experts
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Sharing the experiences of mothers in a virtual group
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Mothers of infants
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Education follow-up
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Message for reminding of educational content together with verbal encouragement
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Sending reminder messages at the end of each week
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Expert’s team
The content and visual validity of the educational program will be measured, and the comments received from the panel of experts. The panel of experts will be included 4 professionals from health education and health promotion field, 3 professionals from the reproductive health and 2 expert from the field of pediatric nurses and a doctor.
Phase II: Implementation of educational intervention
In this step a randomized controlled clinical trial will design to assess the efficacy of prepared protocol. Participants randomly will allocate into two groups. In experimental group we will implement our designed protocol, and control group will not receive any intervention, but they follow as same as experimental group. For ethical issues all educational material will offer them at the end of study.
Study environment and population
This interventional randomized study will be conducted at health centers of Yazd, Iran.
Study sample
This interventional randomized study will be conducted on mothers of infants who have been receiving maternity care at health centers of Yazd, Iran.
According to the study of Araban et al. (14) and considering the level of significance (α = 0.05) and test power (β = 0.8) as well as standard deviation of breastfeeding self-efficacy score which is 4.22 and 4.88 in case and control groups respectively, and in order to achieve a significant difference of at least 2.5 points in the mean score of breastfeeding self-efficacy in the intervention and control groups, and taking into account 10% of probable drop, the sample size is considered to be 57 subjects in each group.
Sampling method
Convenience sampling’s method will apply to select the participants. The sampling method will be random and the participants will be in two groups of intervention and control.
Inclusion criteria
Inclusion criteria include willingness to participate in the study, primiparous mothers, having an under two-years-old infant, physical health of the infant, no underlying disease, access to mobile phones for connecting to virtual space, ability to use internet and media literacy.
Iranian nationality, consent to participate in the study, ability to understand questions or ability to read and write, not participating in any other clinical trials at the same time.
Exclusion criteria
The exclusion criterion is not completing the intervention for any reason and Reluctance to participate in the study.
Data collection method
Quality of Life Questionnaire:
The SF-36 Quality of Life Questionnaire is a general questionnaire for assessing the quality of life of individuals; it assesses the quality of life of individuals in 8 domains of physical function, limitations caused by physical problems, social functioning, physical pain, mental health, limitations caused by mental problems, vitality and general health. The score of each domain is calculated independently and ranges from zero (the worst condition) to 100 (the best condition). Questions of the mentioned dimensions are as follows: physical function (questions 3 to 12); limitation caused by physical problems (13 to 16); social functioning (2, 20 and 32), physical pain (21 and 22), mental health (24 to 28 and 30); limitations caused by mental health problems (17 to 19), vitality (23, 27, 29, 31) and general health (1, 33 to 36). The reliability of this questionnaire has been calculated to be 0.89 and 0.92 by retest and Cronbach's alpha respectively(5).
Breastfeeding Self-efficacy Scale:
Breastfeeding self-efficacy scale is derived from the short form of BSES-SF Dennis. This 14-item scale is designed based on a 5-point Likert scale; so that, I am not sure at all is given score 1, and scores 2 to 5 are given to a bit sure, relatively sure, I am sure, and I am quite sure, respectively. Generally, the range of scores is 14-70, where scores 14-32 indicate low level of self-efficacy, 33-51 moderate self-efficacy, and 52-70 high self-efficacy. This scale has been evaluated psychometrically in the study of Araban et al. and its content and form validities have been confirmed; Cronbach's alpha has also been evaluated to be optimal (0.91) (14).
Evaluation of the infants' anthropometric indices:
Infant's anthropometric indices will be measured using the ratios of infant weight, height, head circumference recorded on the infant's health card or health record in the pre-test and post-test stages.
Data analysis:
We will apply X2 and independent T test to analysis our data by using SPSS version 22.
Outcome measures
Breastfeeding Self efficacy of mothers:
The mean score of Breastfeeding Self efficacy of mothers will be measured using a questionnaire BSES-SF Dennis in the pre-test and post-test phase.
Quality of Life of mothers:
The mean score of Quality of Life of mothers will be measured using a questionnaire SF36 in the pre-test and post test phase.
Infants’ growth status:
Infant's anthropometric indices will be measured using the ratios of infant weight, height, head circumference recorded on the infant's health card or health record in the pre-test and post-test stages.