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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05122390
Other study ID # CcVarmland
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 15, 2022
Est. completion date October 1, 2023

Study information

Verified date October 2023
Source Värmland County Council, Sweden
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

All first-time mothers in Sweden are offered parental support, but local conditions mean that not everyone gets the opportunity to take part in this. Studies show that there is a lack of evidence-based guidelines for the design of parental support in maternal health care. Early labour or latent phase of labour is the part of childbirth were women often feel insecure, in stress and left out from care. First-time mothers who have no experience of one labour before are particularly vulnerable. Many women today use digital applications during pregnancy and in connection with childbirth. There are several digital applications that will help the woman by guiding her and her partner in different decisions about labour, but it is necessary to offer evidence-based, credible electronic and digital solutions for expectant parents. A meta-synthesis from 2018 showed that women use the internet often and the information they receive there has a great influence on their different choices in connection with childbirth. Volume, accessibility, and convenience about digital solutions play a crucial role for women and partners. The digital application Contraction Coper is designed and tested by the company Birth By Heart © in order to facilitate in early labour for the pregnant woman and her partner. The overall purpose of the project is to evaluate whether the application Contraction Coper can contribute to reduced anxiety and stress during pregnancy and childbirth and whether an additional support from a midwife can increase the application use and satisfaction of women when using the application. A randomized controlled trial is planned where first-time mothers after pregnancy week 25 are invited to participation via social platforms. Participating first-time mothers are randomly assigned to one of three groups; experiment group one, which gets access to the application Contraction Coper, experiment group two Contraction Coper Plus which gets access to both the application and support of midwives, so-called "blended" care, or three, the control group offered customary maternity care only. Data collection is conducted using questionnaires, mobile application and activity bracelet.


Description:

The primary outcome is emotional stress in early labour measured with the dimension "Emotional Distress" in the questionnaire Early Labour Experience Questionnaire (ELEQ) Secondary outcomes are Fear of Birth Scale(FOBS), Childbirth Experience Questionnaire (CEQ), used pain relief methods during labour and birth, mode of birth, amount of time used in the application as well as heart rate, sleep and activity for the experimental groups that had activity bracelets in addition.


Recruitment information / eligibility

Status Completed
Enrollment 480
Est. completion date October 1, 2023
Est. primary completion date July 15, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - First time mothers - From pregnancy week 25. - Swedish or English spoken. - Having a Smartphone, Android or Apple application. Exclusion Criteria: °Multiparas.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Contraction Coper
Digital application built on the Birth without fear method, based on four different tools to be used during labour. Breathing, relaxation, voice and mind.
Contraction Coper Plus
Digital application built on the Birth without fear method, based on four different tools to be used during labour. Breathing, relaxation, voice and mind. Clinical guidance from a midwife during two different occasions is added to the group.

Locations

Country Name City State
Sweden County of Värmland Karlstad
Sweden Women's department Karlstad

Sponsors (3)

Lead Sponsor Collaborator
Värmland County Council, Sweden Karlstad University, Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other Labour outcome from medical record Mode of birth; vaginal, vaccuum extraction, cesarean section "At birth"
Other Medical interventions during labour from medical record Amniotomy, oxytocin augmentation yes/no "During labour and birth"
Other Length of labour phases from medical record Length of latent phase, length of active phase, length of pushing phase, measured in minutes and hours "During labour and birth"
Other Pain relif methods used from medical record Nitrus oxide, Epidural, Spinal, non-medical pain relief yes/no "During labour and birth"
Other Apgar Score from medical record Apgar Score ranging from 1-10, at 1 and 5 and 10 minutes after childbirth. Minimum 0-0-0 and maximum 10-10-10. "At birth and during first week after birth"
Other Neonatal outcome from medical record Neonatal care at neonatal intensive unit within one week after childbirth, yes/no "At birth and during first week after birth"
Primary Emotional distress The subscale Emotional distress from Early Labour Experience Questionnaire (ELEQ) will be used for measure. Emotional distress scale is assessed on a five point Likert scale 1-5. Minimum score 6 and maximum score is 30. A higher score represents more distress during early labour. "Group differences at 1 month after birth"
Secondary Fear of birth Fear of forthcoming birth will be measured with Birth scale (FOBS) by a question 'How do you feel right now about the approaching birth?' by placing a mark on two different 10-cm lines, by using the anchors; (a)'calm' and 'worried' and (b) 'no fear' and 'strong fear' creating an average of minimum score is 0 and maximum score 100 with high scores indicating higher levels of childbirth fear. Cut off point is considered at 60. "Assesed during pregnancy week 25 up till week 36 at consent to the study"
Secondary Fear of birth in potential future birth Fear of Birth scale (FOBS) will be used and asked by a question 'How do you feel right now about a potential future birth?' by placing a mark on two different 10-cm lines, by using the anchors; (a)'calm' and 'worried' and (b) 'no fear' and 'strong fear' creating an average of minimum score is 0 and maximum score 100 with high scores indicating higher levels of childbirth fear. Cut off point is considered at 60. Pairwise analyse with score before birth. " Group differencies at 1 month after birth"
Secondary Sense of coherence Sense of Coherence will be measured with SOC-13 (short version). Each question is answered between 1-7. The summed score ranges between 13 and 91. Score is categorized into low(<60), moderate (61-75) and high (>76) SOC. "Assessed during pregnancy week 25 up till week 36 at consent to the study"
Secondary Childbirth experience Childbirth Experience Questionnaire(CEQ) will be used. The questionnaire contains four different dimensions. The items (n=22) are measured on a four point Likert scale. Minimum is 22 and maximum 88. A higher value represents a more positive chidbirth experience. "Group differencies at 1 month after birth"
Secondary Support from birth companion The Birth Companion Support Questionnaire (BCSQ) will be used for measuring the support the woman experiences from her partner during labour and birth and contains two different dimensions. 12 items are answered on a 4 point Likert scale. Minimum is 12 and maximum is 48. A higher score represents a more positive attitude about recieved support. "Group differencies at1 month after birth"
Secondary Childbirth Self-Efficacy Inventory before childbirth The Swedish version of Child Birth Self-efficacy Inventory, (CBSEI) will be used. The questionnaire measuring self-efficacy on both outcome expectancies, i.e. 'what behavior do you think would be useful during labour' as well as self-efficacy expectancies, i.e.' how do you think you will be able to conduct yourselves during labour'. The 15 questions will be asked on ten point Likert scale. ranging from 1 to 10; higher scores indicate a higher degree of childbirth self-efficacy. Minimumscore is 15 and maximum scores are 150 on both scales. "Assessed during pregnancy week 25 up till week 36 at consent to the study"
Secondary Childbirth Self-Efficacy Inventory after childbirth The Swedish version of Child Birth Self-efficacy Inventory (CBSEI) with the assessment of self-efficacy after childbirth. 'How did you conduct yourselves during labour'. The 15 questions will be asked on ten point Likert scale. ranging from 1 to 10; higher scores indicate a higher degree of childbirth self-efficacy during childbirth. Minimumscore is 15 and maximum scores are 150. Pairwise analysis with score before birth for analysis. "Group differencies at1 month after birth"
Secondary Activity bracelet FitBit Heartrate is measured using activity bracelet. A higher heartrate indicates more pain and distress "At the timepoint were contractions starts during early labour and until the baby is born"
Secondary Activity bracelet FitBit Sleep pattern is measured using activity bracelet. A shorter and interrupted sleep indicates more pain and distress "At the timepoint were contractions startsduring early labour and until the baby is born"
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