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Swiss TrAumatic biRth Trial

Improving Mental Health and Physiological Stress Responses in Mothers Following Traumatic Childbirth and in Their Infants: a Randomised Controlled Trial (START)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03576586
Acronym
START
Enrollment
147
Registered
2018-07-03
Start date
2018-08-02
Completion date
2022-02-08
Last updated
2022-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Stress Disorder, Posttraumatic Stress Disorder

Brief summary

This randomized controlled study aims to investigate the effects of a brief computerized intervention (the computer game Tetris) on intrusive memories and other posttraumatic stress symptoms following an emergency cesarean section (ECS). Women who have undergone an emergency cesarian section will be randomly allocated to either the brief computerized intervention plus usual care or an attention placebo control group plus usual care within the first 6 hours following the ECS. Women and their infants will be followed up at ≤ 1 week postpartum, 6 weeks postpartum, and 6 months postpartum. It is predicted that women given the brief computerized intervention will develop fewer intrusive memories and less posttraumatic stress symptoms than those who are not. This will inform the development of a simple computerized early intervention to prevent distressing psychological symptoms after a traumatic event, such as an ECS.

Interventions

Brief computerized intervention (computer game Tetris) plus usual care in the maternity department

Brief cognitive task plus usual care in the maternity department

Sponsors

University of Lausanne
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
University of Fribourg
CollaboratorOTHER
University of Zurich
CollaboratorOTHER
Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Women: * had an ECS at ≥ 34 weeks gestation * gave birth to a live baby * answered with a score of ≥ 2 separately for at least two out of four screening questions regarding perceived threat * gave written consent Partners: * if the woman agrees to participate * was present at the childbirth * gave written consent

Exclusion criteria

Women: * don't speak French sufficiently well to participate in assessments * have an established intellectual disability or psychotic illness * severe illness of mother or infant (e.g. cancer, cardiovascular disease, severe neurodevelopmental difficulties, malformations) * infant requires intensive care * alcohol abuse and/or illegal drug use during pregnancy Partner: \- don't speak French sufficiently well to participate in assessments

Design outcomes

Primary

MeasureTime frameDescription
presence and severity of PTSD symptoms: self-report (mother)6 weeks postpartumPTSD Checklist (PCL-5): subscale and total scores
presence and severity of PTSD symptoms: clinician-rated (mother)6 weeks postpartumClinician-administered PTSD scale (CAPS): subscale and total scores

Secondary

MeasureTime frameDescription
frequency of intrusive traumatic memories (mother)≤ 1 week postpartumtraumatic intrusions diary
presence and severity of ASD symptoms (mother)< 6 hours after ECS, ≤ 1 week postpartumAcute Stress Disorder Scale (ASDS): subscale and total scores
presence and severity of PTSD symptoms: self-report (mother)6 months postpartumPTSD Checklist (PCL-5): subscale and total scores
presence and severity of PTSD symptoms: clinician-rated (mother)6 months postpartumClinician-administered PTSD scale (CAPS): subscale and total scores
presence and severity of anxiety symptoms (mother)< 6 hours after ECS, ≤ 1 week, 6 weeks, 6 months postpartumanxiety subscale of Hospital Anxiety and Depression Scale (HADS): subscale score
sleep time and duration (mother)≤ 1 week postpartumsleep diary
sleep quantity and quality (mother)≤ 1 week, 6 weeks, 6 months postpartumPittsburgh Sleep Quality Index (PSQI): total score
presence and severity of depression symptoms (mother)< 6 hours after ECS, ≤ 1 week, 6 weeks, 6 months postpartumEdinburgh Postnatal Depression Scale (EPDS): total score
sleep and physical activity (mother)≤ 1 week and 6 months postpartumOvernight accelerometer assessments
salivary cortisol: daily profile (mother and infant)≤ 1 week and 6 months postpartumdaily profile
salivary cortisol: stress reactivity (mother and infant)≤ 1 week and 6 months postpartumstress reactivity
heart rate variability: resting state (mother and infant)≤ 1 week and 6 months postpartumresting state
heart rate variability: stress reactivity (mother and infant)≤ 1 week and 6 months postpartumstress reactivity
infant behavior (mother)6 months postpartumInfant Behavior Questionnaire-very short form: total and subscale scores
infant development6 months postpartumBayley Scales of Infant Development (Bayley-III): clinician-rated
mother-infant-bonding (mother)≤ 1 week, 6 weeks, 6 months postpartumMother-to-Infant-Bonding Scale (MIBS): total score
maternal emotional availability6 months postpartumEmotional Availability Scale: clinician-rated

Other

MeasureTime frameDescription
breastfeeding≤ 1 week, 6 weeks, 6 months postpartumbreastfeeding diary and questions
frequency of intrusive traumatic memories (partner)≤ 1 week postpartumtraumatic intrusions diary
Dubowitz neurologic examination (infant)≤ 1 week postpartumstructured clinical examination
presence and severity of PTSD symptoms: clinician-rated (partner)6 weeks, 6 months postpartumClinician-administered PTSD scale (CAPS): subscale and total scores
postnatal perceived stress (mother)6 months postpartumPostnatal Perceived Stress Inventory (PPSI): subscale and total scores
self-reported life events (mother, partner)≤ 1 week and 6 months postpartumLife Events Questionnaire
morningness-eveningness (mother)≤ 1 week postpartumMorningness-Eveningness Questionnaire (MEQ): total score
social support (mother, partner)≤ 1 week, 6 weeks, 6 months postpartumModified Medical Outcomes Study Social Support Survey (MOS-8): total score
couple relationship adjustment (mother, partner)≤ 1 week, 6 weeks, 6 months postpartumRevised Dyadic Adjustment Scale (RDAS): subscale and total scores
parenting stress (mother, partner)6 months postpartumParenting Stress Index - Short Form (PSI-SF): subscale and total scores
post-delivery perceived stress (mother)≤ 1 week postpartumPost-delivery Perceived Stress Inventory (PDPSI): subscale and total scores
presence and severity of PTSD symptoms: self-report (partner)6 weeks, 6 months postpartumPTSD Checklist (PCL-5): subscale and total scores
presence and severity of PTSD symptoms (partner)≤ 1 week postpartumAcute Stress Disorder Scale (ASDS): subscale and total scores
presence and severity of depression symptoms (partner)≤ 1 week, 6 weeks, 6 months postpartumEdinburgh Postnatal Depression Scale (EPDS): total scores
father-infant-bonding (partner)≤ 1 week, 6 weeks, 6 months postpartumMother-to-Infant-Bonding Scale (MIBS): total score
participant feedback questionnaire (mother)< 6 hours after ECSself-report questionnaire
treatment credibility/expectancy questionnaire (mother)< 6 hours after ECSself-report questionnaire
presence and severity of anxiety symptoms (partner)≤ 1 week, 6 weeks, 6 months postpartumanxiety subscale of Hospital Anxiety and Depression Scale (HADS): subscale score
sleep quantity and quality (partner)≤ 1 week, 6 weeks, 6 months postpartumPittsburgh Sleep Quality Index (PSQI): total score

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026