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Evaluation of the Origo prototype for enhancing women's labor & delivery experience.

Evaluation of the Origo prototype for enhancing women's labor & delivery experience.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23730
Enrollment
140
Registered
2012-06-19
Start date
2012-08-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

None listed

Interventions

Origo, an experience design concept that supports the woman during labor in a personal and unobtrusive way by providing real-time breathing support and visualizing progress of labor. ‘Origo’ consists

Sponsors

MMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Maternal age ≥ 18 years; 2. Nulliparae; 3. Singleton pregnancy; 4. Planned vaginal delivery; 5. Gestational age beyond 20 weeks; 6. Dutch speaking.

Exclusion criteria

Exclusion criteria: 1. High patients (tertiary care)-risk; 2. Known fetal anomaly.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure will be maternal quality of life.

Secondary

MeasureTime frame
1. Experiences of the loved ones of the participants; 2. Experiences of the clinical staff; 3. Need for painrelief during labour.

Contacts

Public ContactC. Verhoeven

MMC Veldhoven Postbus 7777

corine.verhoeven@mmc.nl+31 (0)6 48167220

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)