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NCT06068634 Clinical Trial

Patient-Centered Care Survey

Infertility Clinical Trial

— PCCS  

Official title:
Patient-Centered Care Survey of Infertility Patients

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT06068634
Other study ID # FER-CSS-2023-0248
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date October 16, 2023
Est. completion date September 2024

Study information
Verified date September 2023
Source Inception Fertility, LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The key to patient-centered care is to identify what the patient perceives as meaningful. The primary objective of this research is to evaluate which aspects of patient-centered care are priorities to infertility patients, and if those priorities vary by geographical region.

Description:

An electronic survey will be distributed to current patients within The Prelude Network, a network of fertility practices, for a total of six months. Survey responses will be collected anonymously using Survey Monkey. The survey is designed to collect information on patient preferences for patient-centered care. Participants will rank the importance of the different options within each Factor category (Clinic, Physician, Finance, and Staff). In addition, demographic questions are included and will be utilized to determine if these factors could have a significant impact on patient-centered care preferences. It is anticipated that at least 1,000 completed surveys will be collected. A similar survey was distributed to Prelude Network physicians. Patient and physician responses may be compared as part of additional data analysis.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 1000
Est. completion date September 2024
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Study participants must be a current patient within The Prelude Network (a network of fertility clinics) who has had any type of visit at a participating clinic within the last 6 months of the date of study initiation. Exclusion Criteria: Not a current patient at a participating clinic.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Inception Fertility, LLC Houston Texas

Sponsors (2)
Lead Sponsor Collaborator
Inception Fertility, LLC EMD Serono

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparative Analysis Comparative analysis will be conducted. Specifically, the importance of each factor of the Survey Questionnaire data will be analyzed descriptively by summing the ranks given by the patients. Analyses will also be performed by subgroups of patients based on race/ethnicity and other demographic characteristics. 6 months
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