Skip to content

Effectiveness of an E-Learning Training on Addressing Alcohol Use During Pregnancy

Understanding, Supporting, Motivating - Together for an Alcohol-Free Pregnancy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07778251
Acronym
ELAS
Enrollment
268
Registered
2026-08-21
Start date
2024-05-05
Completion date
2025-01-05
Last updated
2026-08-21

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

Conditions

Alcohol Use During Pregnancy

Keywords

Pregnancy, Alcohol Use During Pregnancy, Medical Education, e-learning

Brief summary

A major challenge in health care is equipping health professionals with skills to conduct sensitive conversations which is of importance in the treatment of patients suffering from stigmatized health behaviors such as addiction-related diseases. Alcohol use during pregnancy can cause adverse outcomes for the newborns. Therefore, sensitive conversations with pregnant women conducted by various health professionals who are in contact with them, is of importance. E-learning programs are a good option to teach health professionals with various background how to conduct sensitive conversations, using Motivational Interviewing. The goal of this clinical trial is to learn if the e-learning intervention can improve counseling about alcohol use in pregnancy in heathcare professionals like physicians, midwifes, social workers and others. The main questions it aims to answer is: * Can the e-learning intervention lead to more conversations about alcohol use in pregnancy ? This is being operationalized as follows: Do health professionals address womens' alcohol use more frequently after completion of the e-learning? * Does the e-learning additionally lead to higher values of the following variables (secondary outcomes): knowledge on alcohol use in pregnancy, communication skills, confidence, actual and desired conversation duration? To evaluate these research questions, the study contains two groups: an intervention group receiving the intervention (getting access to the e-learning for four weeks), and a waitlist-control-group which first has a waiting period and later receives the intervention as an incentive. The study has two main measurement point: at baseline (prior to the intervention respectively the waiting period), and after the intervention respectively the waiting period. The waitlist-control group has an additional measurement point after completion of the e-learning. The main hypothesis is that the intervention group shows a higher increase in the alcohol discussion proportion than the waitlist control group (using the measurement point before the e-learning). We therefore expect a significant group-time interaction in the planned repeated-measures ANOVAs for all variables. Participants were asked to complete online questionnaires before assignment to the intervention or waitlist control group and after completing the intervention or the waiting period, respectively. Participants in the intervention group were asked to complete an approximately 8-hour e-learning intervention within four weeks, covering background knowledge on alcohol use during pregnancy and communication skills, including motivational interviewing, with interactive case-based exercises and two assessments. Participants in the waitlist control group received access to the e-learning intervention after a two-month waiting period.

Interventions

An asynchronous interprofessional e-learning program designed to improve knowledge, communication skills, and reflective practice regarding alcohol use during pregnancy and stigma. The program comprises three modules: (1) background knowledge on alcohol use in pregnancy, fetal alcohol spectrum disorders, stigma, and reasons for continued alcohol use; (2) communication skills training based on motivational interviewing principles; and (3) interactive case-based learning. Educational strategies include expert videos, quizzes, reflective exercises addressing personal attitudes and potential stigmatizing beliefs, and twelve interactive patient scenarios. The estimated completion time is approximately eight hours.

Sponsors

University Hospital Tuebingen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Two groups are included: one intervention group and one waitlist-control group. Both groups complete baseline questionnaires, then the intervention group receives the intervention (= gets access to the e-learning platform) and completes questionnaires afterwards. The waitlist control group first has a waiting period, then completes questionnaires again and then receives the intervention as an incentive. Afterwards the control group completes questionnaires again.

Eligibility

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

Inclusion criteria

* Being a physician (gynecologist or obstetrician), midwife, social worker or other health professional working in maternity care * 18 years of age or older * Sufficient German language skills * Internet access

Exclusion criteria

* Not working in the before-named fields * Younger than 18 years of age * Insufficient German language skills * No internet access

Design outcomes

Primary

MeasureTime frameDescription
alcohol discussion proportionAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listDescription: alcohol discussion proportion means the number of pregnant women the health professionals asked about their alcohol consumption in the previous week. To account for different amounts of women seen in a week, the proportion is calculated as a quotient as the number of pregnant women asked about their alcohol use divided by the total number of women seen in the previous week. Both numbers are self-reported by study participants as part of the web-based questionnaires.

Secondary

MeasureTime frameDescription
knowledge on alcohol use in pregnancyAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listself-rated knowledge regarding risks and consequences of alcohol use during pregnancy. The variable is assessed on a 10-point Likert scale (0: no knowledge; 10: very high knowledge). This item was part of the web-based questionnaire.
communication skillsAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listThis outcome describes health professionals' self-rated communication skills in the professional context which means their perceived ability to have effective, sensitive, patient-centered conversation with their patients/clients. This variable is answered on a 4-point Likert scale (1: sufficient; 4 very good). It is also part of the web-based questionnaires.
confidenceAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listThis outcome measure describes health professionals' self-rated confidence in discussing alcohol use during pregnancy with pregnant women they face in their clinical routine. This item is answered on a 4-point Likert scale (1: very unconfident; 4: very confident) and also part of the web-based questionnaires.
actual conversation durationAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listSelf-reported average actual duration (in minutes) of conversations on alcohol use during pregnancy. Also part of the web-based questionnaires.
desired conversation durationAt enrollment and after completion of the e-learning intervention/after 2 months on the waiting listself-reported desired duration (in minutes) on conversation on alcohol use in pregnancy. This should be an indicator of the perceived relevance of the topic. This variable is also assessed as part of the web-based questionnaires.

Countries

Germany

Contacts

PRINCIPAL_INVESTIGATORAnnette Binder, Dr. med.

University Hospital Tübingen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026