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Clinical Trials/NCT06068634
NCT06068634
Completed
Not Applicable

Patient-Centered Care Survey of Infertility Patients

Inception Fertility Research Institute, LLC1 site in 1 country1,500 target enrollmentOctober 23, 2023
ConditionsInfertility

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infertility
Sponsor
Inception Fertility Research Institute, LLC
Enrollment
1500
Locations
1
Primary Endpoint
Descriptive Analysis
Status
Completed
Last Updated
last year

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
October 23, 2023
End Date
April 24, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Inception Fertility Research Institute, LLC
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Current patient within The Prelude Network (a network of fertility clinics).
  • 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.
  • Has not had an appointment within 6 months of the date of study initiation.

Outcomes

Primary Outcomes

Descriptive Analysis

Time Frame: 6 months

Descriptive analyses of survey results.

Study Sites (1)

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