MothersNCT06197100
Supportive Care Training Given to Mothers of Babies With Infants Colic
A study testing Supportive care training in people with Mothers and Infantile Colic, run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).
Trial summary
Infantile Colic is a non-pathological condition that causes babies to cry excessively throughout their first few months of life. It has a prevalence of 15-30% and is defined by excessive sobbing for at least 3 hours per day, 3 days per week for around 3 weeks. Read more about this study
- Who is it for?
- Ages 1 month to 3 monthsHealthy volunteers can take part
- Conditions the study is for
- Mothers, Infantile Colic
- What is being tested?
- Supportive care training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- Mar 2024to Sep 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 month to 3 months
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- Gestational week >37, birth weight >2500g,
- No congenital anomalies related to the digestive system or nutrition,
- Postnatal age of 1-3 months,
- Not receiving colic treatment,
- Diagnosed with Infantile colic by a pediatrician,
- Babies who are exclusively breastfed,
- Mothers of these babies who are over 18 years old, do not use sedative or antiepileptic drugs, can understand and communicate in Turkish, have no mental disabilities, and volunteer to participate in the study will be included in the research.
Who cannot join
- Gestational week ≤ 37 and birth weight ≤ 2500g,
- Those with metabolic disease and congenital anomalies of the digestive system,
- treated for colic,
- not breastfed,
- Babies whose postnatal age is less than 1 month and more than 3 months
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Kirsehir Ahi Evran University
Kirşehi̇r, 40100
Elif Tuba KOÇ, 1, +905063057819 ext. 2908, elif.koc@ahievran.edu.tr
SELİN SÖYÜNMEZ, 2
About this study
Official title: Effectiveness of Supportive Care Training Given to Mothers of Babies With Infant Colic: Randomized Controlled Study
Infantile Colic is a non-pathological condition that causes babies to cry excessively throughout their first few months of life. It has a prevalence of 15-30% and is defined by excessive sobbing for at least 3 hours per day, 3 days per week for around 3 weeks.
Excessive sobbing, blushing, parachroma around the lips, bloating in the abdomen, drawing the legs into the abdomen, coldness at the ends, and fisting of the hands are all symptoms of infantile colic. Another significant clinical aspect of Infantile Colic is its protracted, difficult to soothe, and inexplicable nature. Infantile Colic is thought to have a cicadian pain cycle that begins in the evening.
Read more
Infantile Colic is a non-pathological condition that causes babies to cry excessively throughout their first few months of life. It has a prevalence of 15-30% and is defined by excessive sobbing for at least 3 hours per day, 3 days per week for around 3 weeks.
Excessive sobbing, blushing, parachroma around the lips, bloating in the abdomen, drawing the legs into the abdomen, coldness at the ends, and fisting of the hands are all symptoms of infantile colic. Another significant clinical aspect of Infantile Colic is its protracted, difficult to soothe, and inexplicable nature. Infantile Colic is thought to have a cicadian pain cycle that begins in the evening.
Anxiety and stress that arise during the postpartum period cause a variety of issues in both the mother and the baby, and have a negative impact on the mother-baby bond as well as the mother's care and parenting skills. Sleep deprivation, sleep disturbance, and exhaustion are said to be caused by the sensation of not being able to meet the child's demands. It has been found that as parental stress levels rise, the gut flora deteriorates, and increasing cortisol in breast milk increases the baby's crying attacks. Colic and excessive crying are also risk factors for unfavorable parent-infant interactions. Infantile Colic has been shown to have a negative impact on children's health in the short and long term for all of these reasons. As a result, healthcare experts must devise therapies to lessen the painful impact of Infantile Colic on babies and their families. As a result, the purpose of this study was to see how supportive care training for parents affected the colic levels of babies with Infantile Colic, as well as mothers' perceptions of nursing and parental self-efficacy.
Read the detailed description
Research hypotheses; Supportive care training for mothers of babies with infantile colic H1: Has an effect on the average nursing self-efficacy scores of moms of newborns with infantile colic.
H2: It affects the parental self-efficacy score averages of moms of infantile colic kids, H3: It influences the colic scores of infantile colic babies.
MATERIALS AND METHODS Type of Research Research; It was planned as a pretest-posttest randomized controlled experimental study.
Purpose of the research Research; It was planned to determine the effect of the educational supportive care program for parents on the colic levels of babies with Infantile Colic, the parenting self-efficacy of mothers and the level of mother-infant attachment.
Place and Characteristics of the Research It will be held at the Pediatrics Polyclinic of Kırşehir Ahi Evran University Training and Research Hospital. There are 6 specialist physicians working in the pediatric outpatient clinic.
At the hospital where the research will be conducted, the pediatrician performs a detailed history and physical examination to diagnose infantile colic and identify symptomatic findings. It questions when the crying spells start during the day, tracking the duration of crying, and the baby's behavior. During a complete physical examination, the baby's weight gain, nutrition, defecation pattern, fever and illness are questioned and monitored. Factors that may affect the baby's infantile colic status, such as the baby's diarrhea, eczema, cow's milk protein allergy, lactose intolerance, and mother's smoking, are questioned. In addition, other problems and diseases in the baby's intestines are also questioned. After the history and physical examination are completed by the pediatrician, the baby is diagnosed with infantile colic according to the Rome IV diagnostic criteria.
Design and Blinding This prospective, randomized controlled study is planned to be carried out at Kırşehir Ahi Evran University Training and Research Hospital Pediatrics outpatient clinic between March 2024- August 2024. The study will be conducted based on the CONSORT protocol.
The study population will consist of 1-3 month old babies and their mothers who applied to the Pediatrics outpatient clinic with complaints of restlessness and crying between marc March 2024- August 2024 and were diagnosed with Infantile Colic by the physician, and who meet the research criteria and are selected by randomization. Similar studies were taken into account for the sample of the study. Then, a power analysis will be performed by a statistician using the G*Power program. Thus, the number of samples to be taken into the experimental and control groups will be determined.
Babies and mothers who meet the inclusion criteria will be randomly assigned to experimental and control groups through the online program (http://www.randomizer.org).
Blinding in the study included the parents of the babies included in the study, a pediatrician from the researchers, and a specialist nurse. The first researcher, who only implements the supportive education program, is not blind, so the pre-test post-test evaluation of the study will be collected independently by the second researcher, a specialist nurse. Additionally, the evaluation will be analyzed by an independent statistician. Therefore, the current study will be conducted as a double-blind randomized controlled trial.
Research Inclusion Criteria
- Gestational week >37, birth weight >2500g,
- No congenital anomalies related to the digestive system or nutrition,
- Postnatal age of 1-3 months,
- Not receiving colic treatment,
- Diagnosed with Infantile colic by a pediatrician,
- Babies who are exclusively breastfed,
- Mothers of these babies who are over 18 years old, do not use sedative or antiepileptic drugs, can understand and communicate in Turkish, have no mental disabilities, and volunteer to participate in the study will be included in the research.
Research Exclusion Criteria Babies whose gestational week is ≤ 37 and birth weight ≤ 2500g, who have metabolic diseases and congenital anomalies of the digestive system, who are being treated for colic, who are not breastfed, whose postnatal age is less than 1 month and more than 3 months, and who are under 18 years of age, who do not take antibiotics, sedatives or Mothers who use an antiepileptic type of medication, have communication problems and mental disabilities, and who do not consent to the research will not be included in the study.
Experimental Control Group Matching Criteria of the Research In randomized controlled studies, the number of participants in the groups is expected to be equal or balanced, as well as to be similar in terms of prognostic factors. Therefore, mothers in the experimental and control groups; Babies will be selected similar in terms of age, gender, educational status, marital status and number criteria, and babies will be selected in terms of birth week and birth weight. Stratified randomization will be performed in the study according to these criteria.
Data Collection Tools Data of the research; It will be collected by face-to-face interview with the parent, using the Child and Parent Introduction Form, Breastfeeding Self-Efficacy Scale and Perceived Maternal Parenting Self-Efficacy Scale.
Child and Parent Identification Form This form consists of 4 questions regarding the mother's age, education level, medications used and the baby's birth date.
Breastfeeding Self-Efficacy Scale It is a scale consisting of 33 items developed by Dennis (1999). It consists of two sub-dimensions to determine mothers' breastfeeding skills, beliefs and behaviors regarding breastfeeding. The validity and reliability study of the Turkish form of the scale was conducted by Ekşioğlu and Çeber .
- Technical sub-dimension: It is aimed at determining the mother's breastfeeding skills, such as being able to place the baby on the breast, giving appropriate positioning, recognizing the signs of good breastfeeding, and weaning the baby from the breast.
- Sub-dimension related to personal thoughts: It consists of items including the mother's willingness to feed her baby with breast milk, her belief that she will have milk, not using formula or bottle, and her beliefs and behaviors regarding coping with breastfeeding difficulties.
The scale prepared as a five-point Likert type; I never trust myself, I don't trust myself very much, I sometimes trust myself, I trust myself most of the time, I always trust myself. As the total score on the scale increases, breastfeeding self-efficacy also increases. The lowest score is 33 and the highest score is 165.
Perceived Mother Parenting Self-Efficacy Scale It was developed by Barnes and Adamson-Macedo in 2007 to determine the self-efficacy levels of women who gave birth prematurely. The scale is designed as a four-category scale type; It is an 18-item scale consisting of positive items such as "strongly disagree = 1, disagree = 2, agree = 3, strongly agree = 4". The validity and reliability study of the scale in Turkey was conducted by Verici and Kavlak in 2021. The Cronbach alpha coefficient examined for the internal consistency reliability of the scale was found to be 0.943. A minimum of 18 points and a maximum of 72 points are obtained from the Perceived Mother Parenting Self-Efficacy Scale. An increase in the score obtained indicates that the mother's self-efficacy level increases.
Infant Colic Scale (Appendix-4) The Infant Colic Scale was developed in 2002 by Marsha L. Cirgin Ellet and her colleagues to assist healthcare professionals in diagnosing and evaluating colic. The scale consists of 5 sub-dimensions and 22 questions: Cow's milk/soy protein allergy/intolerance, immature digestive system, immature central nervous system, difficult baby, parent-infant interaction + problematic baby. The Cronbach alpha coefficient of the scale was found to be 0.73.
The validity and reliability study of the scale in Turkey was conducted by Çetinkaya and Başbakkal in 2006. The Cronbach alpha coefficient examined for the internal consistency reliability of the scale was found to be 0.73 (16). The items of the infant colic scale were evaluated on a 6-point Likert scale. Scale items were rated with Likert-type scoring ranging from 1 to 6. The rating was made from 1 (strongly disagree) to 6 (strongly agree). Negative questions were reverse coded for consistency in interpretation of scores. Item 3 in the immature digestive system sub-dimension, items 7, 8, 9 in the immature central nervous system sub-dimension, items 13, 14, 15 in the difficult baby sub-dimension, item in the parent-infant interaction+problem baby sub-dimension. Items 17 and 19 were reverse coded. A low mean score from the scale indicates that colic has decreased, while a high mean score indicates that colic has increased.
Pre-Application A preliminary application will be made with a total of 10 mothers who are not included in the study sample, and the clarity and functionality of the data collection tools will be evaluated. After the preliminary application, necessary corrections will be made to the data collection tools.
APPLICATION Study data will be collected between February 2022 and June 2023. The study group (training group or control group) to which the mothers of infants with infantile colic will be included will be determined by computer using a simple random sampling method. The pre-test of the study will be administered to the experimental and control groups with the Child and Parent Introductory Form, Breastfeeding Self-Efficacy Scale and Perceived Mother Parenting Self-Efficacy Scale before the intervention, and the post-test will be administered immediately and 1 week after the intervention ends.
Supportive care training will be given to the experimental group (Training group). In addition, the booklet prepared by the researchers for the training will be given to the mothers. The supportive care training intervention to be applied to the experimental group is planned to be implemented in 3 modules for 1 week. Interventions will be carried out by the first investigator, a specialist pediatric nurse. Information regarding supportive care training is included in the appendix.
Mothers in the control group will be given an educational brochure containing information on mother-baby nutrition and comforting the baby when crying.
- Conditions
- Mothers, Infantile Colic
- Being tested
- Supportive care training, control grups
- Keywords
- infant, Infantile Colic, support intervention, mothers, Breast Feeding, crying baby
- Medical subject headings
- Colic, Breast Feeding
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Supportive care trainingOther
Also called The researcher will conduct training with the supporting training group and provide them with a booklet that they have created.
The program includes breastfeeding teaching, baby massage, managing gas issues (shaking, white noise), and nutrition for mothers.
control grupsOther
Also called educational brochure
Mothers in this group will be given an educational brochure containing information about colic.
| Study group | Role | What they receive |
|---|---|---|
| supportive care training | Experimental | Training in supportive care will be given to the experimental group (Training group). The mothers will also receive a training booklet from the researchers. The training booklet covers burping newborns, massage, and nourishment for mothers. In addition, mothers will be observed nursing their children, and appropriate breastfeeding instruction will be given if the baby's holding position is a problem. Over the course of a week, the supportive care training intervention will be given in three modules to the experimental group. The interventions will be carried out by the first investigator, a pediatric nursing specialist. Receives: Other: Supportive care training |
| control groups | Active comparator | An educational pamphlet regarding mother-baby nutrition and how to soothe a crying infant will be distributed to mothers in the control group. Receives: Other: control grups |
What is being measured
The primary outcome is the main question the study is designed to answer.
Breastfeeding Self-efficacy
Breastfeeding Self-efficacy Scale: It is a scale consisting of 33 items developed by Dennis (1999). It consists of two sub-dimensions to determine mothers' breastfeeding skills, beliefs and behaviors regarding breastfeeding.
Measured: before intervention/15 days after the intervention
Perceived Maternal Parenting Self-Efficacy
Perceived Maternal Parenting Self-Efficacy Scale: It was created in 2007 by Barnes and Adamson-Macedo to assess the degree of self-efficacy among women who had babies early. The scale yields a minimum of 18 points and a maximum of 72 points. A rise in the score signifies an increase in the mother's degree of self-efficacy.
Measured: before intervention/15 days after the intervention
Infant Colic
The Infant Colic Scale was developed in 2002 by Marsha L. Cirgin Ellet and her colleagues to assist healthcare professionals in diagnosing and evaluating colic. The scale consists of 5 sub-dimensions and 22 questions: Cow's milk/soy protein allergy/intolerance, immature digestive system, immature central nervous system, difficult baby, parent-infant interaction + problem baby.
Measured: before intervention/15 days after the intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jan 2024
- Study startMar 2024 (estimated)
- Primary completionAug 2024 (estimated)
- Study completionSep 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for MothersStudies of the same condition, open and under way.
- More trials run by Kirsehir Ahi Evran UniversitesiThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- there are three sections to it, and they will all be finished simultaneously. This is not a study of drugs or devices. The two arms of the study are Supportive care training, and control groups.
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Kirsehir Ahi Evran Universitesi
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Elif Tuba KOC, Kirsehir Ahi Evran Universitesi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06197100
- Sponsor's protocol ID
- AhiEvranU-UTubaKOÇ-002
- Status last verified
- Dec 2023
- First submitted
- 26 Dec 2023
- Last updated
- 9 Jan 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Despriee AW, Magi CO, Smastuen MC, Glavin K, Nordhagen L, Jonassen CM, Rehbinder EM, Nordlund B, Soderhall C, Carlsen KL, Skjerven HO. Prevalence and perinatal risk factors of parent-reported colic, abdominal pain and other pain or discomforts in infants until 3 months of age - A prospective cohort study in PreventADALL. J Clin Nurs. 2022 Oct;31(19-20):2784-2796. doi: 10.1111/jocn.16097. Epub 2021 Oct 26.
PubMed 34704296Hjern A, Lindblom K, Reuter A, Silfverdal SA. A systematic review of prevention and treatment of infantile colic. Acta Paediatr. 2020 Sep;109(9):1733-1744. doi: 10.1111/apa.15247. Epub 2020 Jun 2.
PubMed 32150292Shirazinia R, Golabchifar AA, Fazeli MR. Efficacy of probiotics for managing infantile colic due to their anti-inflammatory properties: a meta-analysis and systematic review. Clin Exp Pediatr. 2021 Dec;64(12):642-651. doi: 10.3345/cep.2020.01676. Epub 2021 Apr 12.
PubMed 33848417Zeevenhooven J, Browne PD, L'Hoir MP, de Weerth C, Benninga MA. Infant colic: mechanisms and management. Nat Rev Gastroenterol Hepatol. 2018 Aug;15(8):479-496. doi: 10.1038/s41575-018-0008-7.
PubMed 29760502Khajeh M, Sadeghi T, Ramezani M, Derafshi R. Effect of mothers' educational supportive care program on pain intensity and crying duration caused by colic pain in infants aged 1-5 months. Evid Based Care J. 2019;9(1):7-15.
Hechler C, Beijers R, Riksen-Walraven JM, de Weerth C. Are cortisol concentrations in human breast milk associated with infant crying? Dev Psychobiol. 2018 Sep;60(6):639-650. doi: 10.1002/dev.21761. Epub 2018 Jul 1.
PubMed 29961271Ong TG, Gordon M, Banks SS, Thomas MR, Akobeng AK. Probiotics to prevent infantile colic. Cochrane Database Syst Rev. 2019 Mar 13;3(3):CD012473. doi: 10.1002/14651858.CD012473.pub2.
PubMed 30865287Hatch M, Landy K. Do parent training programs reduce crying time in infants with and without colic? Evidence-Based Pract. 2022;25(6):16-7.
Study at a glance
From the registry record, last updated by the sponsor on 9 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of Supportive Care Training Given to Mothers of Babies With Infant Colic: Randomized Controlled Study
- ClinicalTrials.gov ID
- NCT06197100
- Acronym / sponsor ID
- AhiEvranU-UTubaKOÇ-002
- Conditions
- Mothers, Infantile Colic
- Keywords
- infant, Infantile Colic, support intervention, mothers, Breast Feeding, crying baby
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Kirsehir Ahi Evran UniversitesiUniversity, hospital or other
- Study start
- Mar 2024 (estimated)
- Primary completion
- Aug 2024 (estimated)
- Study completion
- Sep 2024 (estimated)
- First posted
- 9 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Infantile Colic is a non-pathological condition that causes babies to cry excessively throughout their first few months of life. It has a prevalence of 15-30% and is defined by excessive sobbing for at least 3 hours per day, 3 days per week for around 3 weeks.
Excessive sobbing, blushing, parachroma around the lips, bloating in the abdomen, drawing the legs into the abdomen, coldness at the ends, and fisting of the hands are all symptoms of infantile colic. Another significant clinical aspect of Infantile Colic is its protracted, difficult to soothe, and inexplicable nature. Infantile Colic is thought to have a cicadian pain cycle that begins in the evening.
Infantile Colic is a non-pathological condition that causes babies to cry excessively throughout their first few months of life. It has a prevalence of 15-30% and is defined by excessive sobbing for at least 3 hours per day, 3 days per week for around 3 weeks.
Excessive sobbing, blushing, parachroma around the lips, bloating in the abdomen, drawing the legs into the abdomen, coldness at the ends, and fisting of the hands are all symptoms of infantile colic. Another significant clinical aspect of Infantile Colic is its protracted, difficult to soothe, and inexplicable nature. Infantile Colic is thought to have a cicadian pain cycle that begins in the evening.
Anxiety and stress that arise during the postpartum period cause a variety of issues in both the mother and the baby, and have a negative impact on the mother-baby bond as well as the mother's care and parenting skills. Sleep deprivation, sleep disturbance, and exhaustion are said to be caused by the sensation of not being able to meet the child's demands. It has been found that as parental stress levels rise, the gut flora deteriorates, and increasing cortisol in breast milk increases the baby's crying attacks. Colic and excessive crying are also risk factors for unfavorable parent-infant interactions. Infantile Colic has been shown to have a negative impact on children's health in the short and long term for all of these reasons. As a result, healthcare experts must devise therapies to lessen the painful impact of Infantile Colic on babies and their families. As a result, the purpose of this study was to see how supportive care training for parents affected the colic levels of babies with Infantile Colic, as well as mothers' perceptions of nursing and parental self-efficacy.
Detailed description
Research hypotheses; Supportive care training for mothers of babies with infantile colic H1: Has an effect on the average nursing self-efficacy scores of moms of newborns with infantile colic.
H2: It affects the parental self-efficacy score averages of moms of infantile colic kids, H3: It influences the colic scores of infantile colic babies.
MATERIALS AND METHODS Type of Research Research; It was planned as a pretest-posttest randomized controlled experimental study.
Purpose of the research Research; It was planned to determine the effect of the educational supportive care program for parents on the colic levels of babies with Infantile Colic, the parenting self-efficacy of mothers and the level of mother-infant attachment.
Place and Characteristics of the Research It will be held at the Pediatrics Polyclinic of Kırşehir Ahi Evran University Training and Research Hospital. There are 6 specialist physicians working in the pediatric outpatient clinic.
At the hospital where the research will be conducted, the pediatrician performs a detailed history and physical examination to diagnose infantile colic and identify symptomatic findings. It questions when the crying spells start during the day, tracking the duration of crying, and the baby's behavior. During a complete physical examination, the baby's weight gain, nutrition, defecation pattern, fever and illness are questioned and monitored. Factors that may affect the baby's infantile colic status, such as the baby's diarrhea, eczema, cow's milk protein allergy, lactose intolerance, and mother's smoking, are questioned. In addition, other problems and diseases in the baby's intestines are also questioned. After the history and physical examination are completed by the pediatrician, the baby is diagnosed with infantile colic according to the Rome IV diagnostic criteria.
Design and Blinding This prospective, randomized controlled study is planned to be carried out at Kırşehir Ahi Evran University Training and Research Hospital Pediatrics outpatient clinic between March 2024- August 2024. The study will be conducted based on the CONSORT protocol.
The study population will consist of 1-3 month old babies and their mothers who applied to the Pediatrics outpatient clinic with complaints of restlessness and crying between marc March 2024- August 2024 and were diagnosed with Infantile Colic by the physician, and who meet the research criteria and are selected by randomization. Similar studies were taken into account for the sample of the study. Then, a power analysis will be performed by a statistician using the G*Power program. Thus, the number of samples to be taken into the experimental and control groups will be determined.
Babies and mothers who meet the inclusion criteria will be randomly assigned to experimental and control groups through the online program (http://www.randomizer.org).
Blinding in the study included the parents of the babies included in the study, a pediatrician from the researchers, and a specialist nurse. The first researcher, who only implements the supportive education program, is not blind, so the pre-test post-test evaluation of the study will be collected independently by the second researcher, a specialist nurse. Additionally, the evaluation will be analyzed by an independent statistician. Therefore, the current study will be conducted as a double-blind randomized controlled trial.
Research Inclusion Criteria
- Gestational week >37, birth weight >2500g,
- No congenital anomalies related to the digestive system or nutrition,
- Postnatal age of 1-3 months,
- Not receiving colic treatment,
- Diagnosed with Infantile colic by a pediatrician,
- Babies who are exclusively breastfed,
- Mothers of these babies who are over 18 years old, do not use sedative or antiepileptic drugs, can understand and communicate in Turkish, have no mental disabilities, and volunteer to participate in the study will be included in the research.
Research Exclusion Criteria Babies whose gestational week is ≤ 37 and birth weight ≤ 2500g, who have metabolic diseases and congenital anomalies of the digestive system, who are being treated for colic, who are not breastfed, whose postnatal age is less than 1 month and more than 3 months, and who are under 18 years of age, who do not take antibiotics, sedatives or Mothers who use an antiepileptic type of medication, have communication problems and mental disabilities, and who do not consent to the research will not be included in the study.
Experimental Control Group Matching Criteria of the Research In randomized controlled studies, the number of participants in the groups is expected to be equal or balanced, as well as to be similar in terms of prognostic factors. Therefore, mothers in the experimental and control groups; Babies will be selected similar in terms of age, gender, educational status, marital status and number criteria, and babies will be selected in terms of birth week and birth weight. Stratified randomization will be performed in the study according to these criteria.
Data Collection Tools Data of the research; It will be collected by face-to-face interview with the parent, using the Child and Parent Introduction Form, Breastfeeding Self-Efficacy Scale and Perceived Maternal Parenting Self-Efficacy Scale.
Child and Parent Identification Form This form consists of 4 questions regarding the mother's age, education level, medications used and the baby's birth date.
Breastfeeding Self-Efficacy Scale It is a scale consisting of 33 items developed by Dennis (1999). It consists of two sub-dimensions to determine mothers' breastfeeding skills, beliefs and behaviors regarding breastfeeding. The validity and reliability study of the Turkish form of the scale was conducted by Ekşioğlu and Çeber .
- Technical sub-dimension: It is aimed at determining the mother's breastfeeding skills, such as being able to place the baby on the breast, giving appropriate positioning, recognizing the signs of good breastfeeding, and weaning the baby from the breast.
- Sub-dimension related to personal thoughts: It consists of items including the mother's willingness to feed her baby with breast milk, her belief that she will have milk, not using formula or bottle, and her beliefs and behaviors regarding coping with breastfeeding difficulties.
The scale prepared as a five-point Likert type; I never trust myself, I don't trust myself very much, I sometimes trust myself, I trust myself most of the time, I always trust myself. As the total score on the scale increases, breastfeeding self-efficacy also increases. The lowest score is 33 and the highest score is 165.
Perceived Mother Parenting Self-Efficacy Scale It was developed by Barnes and Adamson-Macedo in 2007 to determine the self-efficacy levels of women who gave birth prematurely. The scale is designed as a four-category scale type; It is an 18-item scale consisting of positive items such as "strongly disagree = 1, disagree = 2, agree = 3, strongly agree = 4". The validity and reliability study of the scale in Turkey was conducted by Verici and Kavlak in 2021. The Cronbach alpha coefficient examined for the internal consistency reliability of the scale was found to be 0.943. A minimum of 18 points and a maximum of 72 points are obtained from the Perceived Mother Parenting Self-Efficacy Scale. An increase in the score obtained indicates that the mother's self-efficacy level increases.
Infant Colic Scale (Appendix-4) The Infant Colic Scale was developed in 2002 by Marsha L. Cirgin Ellet and her colleagues to assist healthcare professionals in diagnosing and evaluating colic. The scale consists of 5 sub-dimensions and 22 questions: Cow's milk/soy protein allergy/intolerance, immature digestive system, immature central nervous system, difficult baby, parent-infant interaction + problematic baby. The Cronbach alpha coefficient of the scale was found to be 0.73.
The validity and reliability study of the scale in Turkey was conducted by Çetinkaya and Başbakkal in 2006. The Cronbach alpha coefficient examined for the internal consistency reliability of the scale was found to be 0.73 (16). The items of the infant colic scale were evaluated on a 6-point Likert scale. Scale items were rated with Likert-type scoring ranging from 1 to 6. The rating was made from 1 (strongly disagree) to 6 (strongly agree). Negative questions were reverse coded for consistency in interpretation of scores. Item 3 in the immature digestive system sub-dimension, items 7, 8, 9 in the immature central nervous system sub-dimension, items 13, 14, 15 in the difficult baby sub-dimension, item in the parent-infant interaction+problem baby sub-dimension. Items 17 and 19 were reverse coded. A low mean score from the scale indicates that colic has decreased, while a high mean score indicates that colic has increased.
Pre-Application A preliminary application will be made with a total of 10 mothers who are not included in the study sample, and the clarity and functionality of the data collection tools will be evaluated. After the preliminary application, necessary corrections will be made to the data collection tools.
APPLICATION Study data will be collected between February 2022 and June 2023. The study group (training group or control group) to which the mothers of infants with infantile colic will be included will be determined by computer using a simple random sampling method. The pre-test of the study will be administered to the experimental and control groups with the Child and Parent Introductory Form, Breastfeeding Self-Efficacy Scale and Perceived Mother Parenting Self-Efficacy Scale before the intervention, and the post-test will be administered immediately and 1 week after the intervention ends.
Supportive care training will be given to the experimental group (Training group). In addition, the booklet prepared by the researchers for the training will be given to the mothers. The supportive care training intervention to be applied to the experimental group is planned to be implemented in 3 modules for 1 week. Interventions will be carried out by the first investigator, a specialist pediatric nurse. Information regarding supportive care training is included in the appendix.
Mothers in the control group will be given an educational brochure containing information on mother-baby nutrition and comforting the baby when crying.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
- Model description
- there are three sections to it, and they will all be finished simultaneously. This is not a study of drugs or devices. The two arms of the study are Supportive care training, and control groups.
| Arm | Type | Receives |
|---|---|---|
| supportive care training | Experimental | Other: Supportive care trainingTraining in supportive care will be given to the experimental group (Training group). The mothers will also receive a training booklet from the researchers. The training booklet covers burping newborns, massage, and nourishment for mothers. In addition, mothers will be observed nursing their children, and appropriate breastfeeding instruction will be given if the baby's holding position is a problem. Over the course of a week, the supportive care training intervention will be given in three modules to the experimental group. The interventions will be carried out by the first investigator, a pediatric nursing specialist. |
| control groups | Active comparator | Other: control grupsAn educational pamphlet regarding mother-baby nutrition and how to soothe a crying infant will be distributed to mothers in the control group. |
Who may qualify
- Ages
- 1 month to 3 months
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (7 listed)
- Gestational week >37, birth weight >2500g,
- No congenital anomalies related to the digestive system or nutrition,
- Postnatal age of 1-3 months,
- Not receiving colic treatment,
- Diagnosed with Infantile colic by a pediatrician,
Key exclusion criteria (5 listed)
- Gestational week ≤ 37 and birth weight ≤ 2500g,
- Those with metabolic disease and congenital anomalies of the digestive system,
- treated for colic,
- not breastfed,
- Babies whose postnatal age is less than 1 month and more than 3 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Supportive care trainingAlso: The researcher will conduct training with the supporting training group and provide them with a booklet that they have created.The program includes breastfeeding teaching, baby massage, managing gas issues (shaking, white noise), and nutrition for mothers. | Other | supportive care training |
| control grupsAlso: educational brochureMothers in this group will be given an educational brochure containing information about colic. | Other | control groups |
Primary outcome
Breastfeeding Self-efficacy
Time frame: before intervention/15 days after the intervention
Breastfeeding Self-efficacy Scale: It is a scale consisting of 33 items developed by Dennis (1999). It consists of two sub-dimensions to determine mothers' breastfeeding skills, beliefs and behaviors regarding breastfeeding.
Perceived Maternal Parenting Self-Efficacy
Time frame: before intervention/15 days after the intervention
Perceived Maternal Parenting Self-Efficacy Scale: It was created in 2007 by Barnes and Adamson-Macedo to assess the degree of self-efficacy among women who had babies early. The scale yields a minimum of 18 points and a maximum of 72 points. A rise in the score signifies an increase in the mother's degree of self-efficacy.
Infant Colic
Time frame: before intervention/15 days after the intervention
The Infant Colic Scale was developed in 2002 by Marsha L. Cirgin Ellet and her colleagues to assist healthcare professionals in diagnosing and evaluating colic. The scale consists of 5 sub-dimensions and 22 questions: Cow's milk/soy protein allergy/intolerance, immature digestive system, immature central nervous system, difficult baby, parent-infant interaction + problem baby.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Jan 2024.
- Background: PubMed 34704296Despriee AW, Magi CO, Smastuen MC, Glavin K, Nordhagen L, Jonassen CM, Rehbinder EM, Nordlund B, Soderhall C, Carlsen KL, Skjerven HO. Prevalence and perinatal risk factors of parent-reported colic, abdominal pain and other pain or discomforts in infants until 3 months of age - A prospective cohort study in PreventADALL. J Clin Nurs. 2022 Oct;31(19-20):2784-2796. doi: 10.1111/jocn.16097. Epub 2021 Oct 26.
- Background: PubMed 32150292Hjern A, Lindblom K, Reuter A, Silfverdal SA. A systematic review of prevention and treatment of infantile colic. Acta Paediatr. 2020 Sep;109(9):1733-1744. doi: 10.1111/apa.15247. Epub 2020 Jun 2.
- Background: PubMed 33848417Shirazinia R, Golabchifar AA, Fazeli MR. Efficacy of probiotics for managing infantile colic due to their anti-inflammatory properties: a meta-analysis and systematic review. Clin Exp Pediatr. 2021 Dec;64(12):642-651. doi: 10.3345/cep.2020.01676. Epub 2021 Apr 12.
- Background: PubMed 29760502Zeevenhooven J, Browne PD, L'Hoir MP, de Weerth C, Benninga MA. Infant colic: mechanisms and management. Nat Rev Gastroenterol Hepatol. 2018 Aug;15(8):479-496. doi: 10.1038/s41575-018-0008-7.
- BackgroundKhajeh M, Sadeghi T, Ramezani M, Derafshi R. Effect of mothers' educational supportive care program on pain intensity and crying duration caused by colic pain in infants aged 1-5 months. Evid Based Care J. 2019;9(1):7-15.
- Background: PubMed 29961271Hechler C, Beijers R, Riksen-Walraven JM, de Weerth C. Are cortisol concentrations in human breast milk associated with infant crying? Dev Psychobiol. 2018 Sep;60(6):639-650. doi: 10.1002/dev.21761. Epub 2018 Jul 1.
- Background: PubMed 30865287Ong TG, Gordon M, Banks SS, Thomas MR, Akobeng AK. Probiotics to prevent infantile colic. Cochrane Database Syst Rev. 2019 Mar 13;3(3):CD012473. doi: 10.1002/14651858.CD012473.pub2.
- BackgroundHatch M, Landy K. Do parent training programs reduce crying time in infants with and without colic? Evidence-Based Pract. 2022;25(6):16-7.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kirsehir Ahi Evran University
Kirşehi̇r, Turkey (Türkiye)
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Supportive care training in people with Mothers and Infantile Colic, run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 9 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Breastfeeding Self-efficacy (time frame: before intervention/15 days after the intervention). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06197100, which also lists 8 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2024.