Labour Pain Relief Options: Video Versus Pamphlet for Easing Fear of Birth and Improving Preparedness in Pregnant Patients, an RCT

ConditionLabour Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age19+
SponsorFraser Health

About this trial

The goal of this clinical trial is to investigate whether a structured educational video improves outcomes related to fear of birth and patient preparedness for pregnant adults who are planning to labour.

The primary objective is to evaluate whether an educational video can reduce fear of childbirth more effectively than a pamphlet.

Patients will complete a baseline questionnaire assessing their knowledge of labour pain relief options and their current fear of childbirth. The control group will be provided an electronic version of a pamphlet while the intervention group will watch an educational video outlining pharmacologic and non-pharmacologic options for labour pain relief. Immediately after the intervention, all participants will complete the same questionnaire to assess changes in fear and knowledge.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults age 19 years and over

Primiparous patients over 32 weeks of gestation

Planning to labour

Disqualifiers

Emergency delivery/already in labour

Patients who are not intending to labour

Unable to give consent

Unable to communicate in English

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pamphlet

    Behavioral

    Electronic version of pamphlet with comprehensive and up-to-date content on both pharmacologic and non-pharmacologic pain relief options during labour.

  • Video

    Behavioral

    An educational video featuring anesthesiologists explaining both pharmacologic and non-pharmacologic pain relief options

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: PamphletActive comparator 1 intervention
Group B: VideoExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in fear of birth (FOB)

The primary outcome is the change in fear of birth (FOB), as assessed immediately after reviewing the educational material using a two-item visual analog scale. The FOB total score is derived by calculating the average of the two items that assess fear and worry regarding the upcoming birth, each ranging from 0 to 100, with higher scores indicating higher FOB.

Time frame
From enrollment to end of post-intervention questionnaire (same day)

Secondary outcomes

1

Change in fear and worry scores

Time frame
From enrollment to end of post-intervention questionnaire (same day)
2

Changes in knowledge about pain relief options

Time frame
From enrollment to end of post-intervention questionnaire (same day)
3

Birth satisfaction

Time frame
From enrollment to end of follow-up (2 weeks post estimated delivery date)
4

Type of analgesia used during labour

Time frame
From enrollment to end of follow-up (2 weeks post estimated delivery date)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: