- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07568834
Impact of Pelvic Pain Podcast
May 15, 2026 updated by: Lara Harvey, Vanderbilt University Medical Center
"Impact of an Educational Podcast for Patients With Chronic Pelvic Pain"
The purpose of this research study is to study the impact of an educational podcast on pelvic pain.
If you decide to take part in this research, you may receive the standard treatment for pelvic pain, or you may receive the standard treatment plus access to an educational podcast series.
You will be randomly assigned to receive access to the podcast or to receive standard care.
If you are assigned to receive access to the podcast, participating in this research will involve listening to a podcast series.
All participants will complete three ten-minute online surveys over the course of 6 months.
Reasons you may choose to participate in this research are if you want to learn more about pelvic pain and possible benefits of listening to the podcast, such as improved quality of life, reduced stigma, or increased satisfaction with your medical care.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Annie N Apple, MD
- Phone Number: 484-320-0710
- Email: annie.apple@vumc.org
Study Locations
-
-
Tennessee
-
Nashville, Tennessee, United States, 37204
- Recruiting
- Vanderbilt Center for Women's Health
-
Contact:
- Annie Apple, MD
- Phone Number: 484-320-0710
- Email: annie.apple@vumc.org
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being seen as a new patient or consult visit by provider in the division of minimally invasive gynecology surgery for chronic pelvic pain or endometriosis
- 18 years of age or older
- Understand English
- Has an email address and personal device with capability to listen to an audio podcast
Exclusion Criteria:
- Not able to speak English
- Being seen for acute pelvic pain
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Podcast
Podcast Series - 12 episodes on topics related to chronic pelvic pain
|
Audio podcast on chronic pelvic pain topics
|
|
No Intervention: Standard Care
Standard care for pelvic pain, no access to podcast
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Support Subset of Endometriosis Health Profile 30
Time Frame: 6 months
|
6 months
|
|
|
Pelvic Pain Impact Questionnaire
Time Frame: 6 months
|
Score range: Typically transformed to 0-100 Interpretation:
|
6 months
|
|
Loneliness and Social Isolation, DeJong Gierveld Loneliness Scale
Time Frame: 6 months
|
Score range: 0-6 Interpretation:
|
6 months
|
|
Chronic Illness Anticipated Stigma Scale
Time Frame: 6 months
|
Score range: 12-60 Interpretation:
|
6 months
|
|
Patient Satisfaction CSQ4 Questionnaire
Time Frame: 6 months
|
Score range: 4-16 Interpretation:
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Experience with Podcast
Time Frame: 6 months
|
Asks about usability and feedback
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Amador FLD, Alves GCG, Santos VRD, Moreira RSL. Use of podcasts for health education: a scoping review. Rev Bras Enferm. 2024 Mar 15;77(1):e20230096. doi: 10.1590/0034-7167-2023-0096. eCollection 2024.
- De Corte P, Klinghardt M, von Stockum S, Heinemann K. Time to Diagnose Endometriosis: Current Status, Challenges and Regional Characteristics-A Systematic Literature Review. BJOG. 2025 Jan;132(2):118-130. doi: 10.1111/1471-0528.17973. Epub 2024 Oct 7.
- Calvi C, Sherman KA, Pham D. Loneliness and Perceived Social Support in Endometriosis: The Roles of Body Image Disturbance and Anticipated Stigma. Int J Behav Med. 2024 Jun;31(3):433-444. doi: 10.1007/s12529-023-10230-w. Epub 2023 Oct 26.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 5, 2026
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
August 1, 2027
Study Registration Dates
First Submitted
April 28, 2026
First Submitted That Met QC Criteria
April 28, 2026
First Posted (Actual)
May 6, 2026
Study Record Updates
Last Update Posted (Actual)
May 19, 2026
Last Update Submitted That Met QC Criteria
May 15, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 251820
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Research data available upon request and will include de-identified survey responses
IPD Sharing Time Frame
After completion of the study
IPD Sharing Access Criteria
Those who request the data for research purposes, can be sent in a secure electronic fashion upon request and review
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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