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Rapid Prototyping Models for Patient Education

Use of 3-D Printed Models to Improve Patient Understanding During the Informed Consent Process: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02718807
Enrollment
20
Registered
2016-03-24
Start date
2016-05-31
Completion date
2017-01-31
Last updated
2022-02-11

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

Conditions

Patient Education

Keywords

Patient Care, Education

Brief summary

Pre-made rapid prototyping models will be used to increase patient education versus current methodologies.

Detailed description

Post-partum women and their co-parent will have a medical condition explained to them first verbally, followed by a questionnaire, and then with the use of anatomical models created by rapid prototyping, followed by a questionnaire. The two questionnaires will then be compared.

Interventions

OTHERRP model explanation and questionnaire

Rapid prototyping models of anatomy will be used to demonstrate an anatomic and medical condition and participants will grade the experience on a questionnaire.

Sponsors

Milton S. Hershey Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Mother * Post-partum * Atraumatic delivery of healthy, live infant at HMC * Age \> 18 Co-parent * Co-parent * Atraumatic delivery of healthy, live infant at HMC * Age \> 18

Exclusion criteria

* any pregnancy related issues * fetal loss * NICU stay \> 6 hours * Emergent cesarean section * Post-partum hemorrhage * Hysterectomy * Any other condition requiring unplanned, medical intervention during labor and delivery * Prior fetal loss or anomaly * Inability to read or write English * those who do not consent

Design outcomes

Primary

MeasureTime frame
Difference in questionnaire scorethrough study completion, an average of 1 year

Secondary

MeasureTime frame
Participant Agethrough study completion, an average of 1 year
Participant Education Levelthrough study completion, an average of 1 year
Participant Genderthrough study completion, an average of 1 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026