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Evaluation of the Origo prototype for enhancing women*s labor & delivery experience. A pilot study.

Evaluation of the Origo prototype for enhancing women*s labor & delivery experience. A pilot study. - Origo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37102
Enrollment
120
Registered
2012-12-13
Start date
2013-02-05
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

child birth experience

Interventions

Origo concept, existing of an app for the Ipod

Sponsors

Philips Design
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Maternal age * 18 years -Nulliparae -Singleton pregnancy -Planned vaginal delivery -Gestational age beyond 20 weeks -Dutch speaking -Informed consent

Exclusion criteria

Exclusion criteria: -High patients (tertiary care)-risk -Known fetal anomaly

Design outcomes

Primary

MeasureTime frame
To gain an estimate of the effect size (in means of improvement/change in maternal quality of life), as well as an estimate of the variability in our measures. (feasibility study)

Secondary

MeasureTime frame
Secondary Objectives: Secondary objective of this study is to gain insights into the value of the proposition *Origo* for women and their partners and/or relatives, medical staff and care institution. This entails the following sub objectives: - Gain a deep understanding of how this concept influences the woman*s experiences before, during and after giving birth: most important secondary objective is maternal quality of life - Understand how this concept is used in practice by the different stakeholders - Investigate how it affects the clinical workflow in and around the delivery rooms - Gather feedback on proposition for future development and improvement

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)