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A single-blind randomized controlled trial to study the effects of a labor guide on perceived control in labor. The experimental arm will receive an evidence-based labor guide at the time of admission for scheduled induction of labor. The control arm will receive the standard of care in-person counseling regarding options for labor interventions
Participants will be randomized to receive an evidence-based labor guide at the time of admission for scheduled induction of labor, or the standard of care. Following delivery, patients will be surveyed about their labor experience. Chart review will be done to collect data on obstetric interventions and outcomes and neonatal outcomes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental Group | Experimental | Participants will receive an evidence-based labor guide at the time of admission for scheduled induction of labor |
|
| Control Group | No Intervention | Participants will receive the standard of care in-person counseling regarding options for labor interventions. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| evidence-based labor guide | Other | Participants will be provided with written education about potential complications and interventions. Information will be provided at the time of admission for labor induction. |
| Measure | Description | Time Frame |
|---|---|---|
| Labor Agentry Scale-10 (LAS-10) | A validated questionnaire that measures patient-perceived control during labor | 1-7 days following delivery |
| Measure | Description | Time Frame |
|---|---|---|
| Labor Interventions | Whether patients received labor interventions including Pitocin, misoprostol, cook balloon, intra-uterine pressure catheter, manual rotation | During labor |
| Maternal hyper/hypotension |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Women's Health Research Unit Department of Ob/Gyn | Contact | 503-494-3666 | whru@ohsu.edu |
| Name | Affiliation | Role |
|---|---|---|
| Fei Cai, MD | Oregon Health and Science University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Oregon Health and Science University | Recruiting | Portland | Oregon | 97239 | United States |
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1:1 randomization will be done using REDCap.
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Whether the patient experience hypertension or hypotension
| During induction of labor |
| Intrapartum blood loss | The amount of blood loss a patient experienced during delivery | Labor and delivery |
| Cesarean section | Whether a patient requires a cesarean delivery | Delivery |
| Time to delivery | The duration from admission for induction to delivery | Admission for induction to delivery |