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NCT04283721
Optimal Method and Timing to Provide Information on Epidural and Spinal Anaesthesia for Primiparas
NA trial testing Educational video in Patient Satisfaction in 280 participants. Status unknown.
28 June 2021
Quick facts
| Lead sponsor | Sligo General Hospital |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | single group |
| Masking | double |
| Primary purpose | other |
| Enrollment | 280 |
| Start date | 2 March 2020 |
| Primary completion | 28 June 2021 |
| Estimated completion | 28 June 2021 |
Drugs / interventions tested
- Educational video
Conditions studied
- Patient Satisfaction — all drugs for Patient Satisfaction →
- Confidence, Self — all drugs for Confidence, Self →
Sponsor
Sligo General Hospital
Who can join
18 and older, female only, with Patient Satisfaction or Confidence, Self. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Expectant mothers can give birth to their child either by vaginal delivery or by a caesarean section (the latter can be planned or necessary during an emergency). Among the pain-relieving options for vaginal delivery, they can choose to receive epidural analgesia. In case of a caesarean section, the three anaesthetic options are epidural, spinal, or general anaesthesia. The current Irish standard of care for the provision of information and consent for epidural and spinal anaesthesia entails a consultation with the anaesthesiologists at the request of the expectant mothers, shortly before the procedure. The uniformity of the information provided with this method is being debated. Moreover, there is a lack of consensus on the best timing and setting to informing patients. With the aim of standardising the provision of information on epidural and spinal anaesthesia, the Anaesthetic Department in Sligo University Hospital has created an informational video on such procedures, in which all benefits and possible complications are explained in detail. This video can be shown to expectant mothers at the antenatal classes or in the early stage of labour, as soon as they present to the labour ward. Importantly, this video is not aimed at promoting the use of the epidural catheter, rather at providing expectant mothers all the information on the technique, benefits, side effects and possible complications of the procedure. The main objective of this study is to evaluate whether this informational video is effective in improving patient confidence and satisfaction regarding these pain-relieving options, and what is the optimal timing to show the video. Our hypothesis is that, compared to the control group, women who watch the informational video will feel more confident in choosing to receive or not these pain-relieving options and therefore have a more positive childbirth experience. This study is a randomised control trial. Randomisation will produce 4 groups in total. Depending on the group allocation, participants may or may not be shown the informational video in relation to spinal/epidural anaesthesia at various stages (antenatal classes or at the time of their arrival on the labour ward). The control group will receive the usual Irish standard of care. After delivery, the patients will be interviewed with a questionnaire that will explore: * Their satisfaction with the information provided in relation to the epidural/spinal anaesthesia; * Their confidence in choosing to receive/not to receive these pain relieving options; * Their ability to recollect the information provided on these pain-relieving options. To the extent of our knowledge, this is the first study that aims at improving parturients' sense of confidence and satisfaction in relation to the information provided on epidural and spinal anaesthesia. Should patients find this means of information beneficial to their care and overall experience, there is potential for nationwide distribution.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04283721 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sligo General Hospital
- Last refreshed: 25 February 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04283721.
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