The PelvicSense Turnkey Workflow 

From Referral to Results in 5 Automated Steps 

Implementing neuroplastic pain-science-informed self-management to improve 90-day functional outcomes for people with chronic pelvic pain.
Requires less than 5 minutes of clinical workflow time. No complex EHR integration needed

Step 1:

Patient Identification

The provider identifies candidates with chronic pelvic pain or related dysfunction.

  • Chronic Pelvic Pain (CPP) & PFD

  • Overactive Bladder (OAB) & Interstitial Cystitis (IC)

  • Irritable Bowel Syndrome (IBS)

  • Vulvodynia & Pudendal Neuralgia

  • Check patient comfort with digital tools and English proficiency.

 

Step 2:

After-Visit Referral

The provider integrates the program into the existing clinical workflow.

  • Embed Secure HIPAA Jotform links

  • Include PelvicSense flyer links

  • Insert into After-Visit Summary (AVS)

  • Send via Patient Portal message

  • Implementation requires <5 minutes of clinical time.

Step 3:

Assessment + Activation

The patient begins their journey with clinical baseline metrics collected via secure, HIPAA-compliant Jotform.

  • Complete PEG & PCS assessments

  • Encrypted data transmission (Non-PHI)

  • Immediate PelvicSense curriculum activation

  • Automated provider notification

  • Securely hosted, privacy-first patient intake. 

 

Step 4:

Automated 90-Day Follow-Up

The system manages long-term tracking without staff intervention.

  • Scheduled reassessment emails

  • Engagement "nudges" included

  • 90-day follow-up Q's completed

  • Consistent support touchpoints

  • Zero manual follow-up required.

 

Step 5:

Outcomes Reporting

Actionable data delivered directly to the clinical team.

  • Pain level (#) change analysis

  • Catastrophizing reduction data

  • Individual patient progress PDF

  • Total pilot outcome summary

  • Validated metrics for documentation.

 

Master Clinician Oversight

Developed by a Master Clinician Pelvic PT with over 25 years of specialization in complex chronic pelvic pain and desensitization protocols

Proven Pilot Results

Initial pilot data demonstrates significant 3-point reductions in  Pain Intensity and reduced  Catastastrophizing (PCS) scores across diverse pelvic participants

Evidence-Based Validation

Efficacy is being evaluated via an active Randomized Controlled Trial (RCT), ensuring the  curriculum meets the highest clinical standards

Federal-Grade Vetting

Currently in the Veterans Administration (VA) procurement pipeline for system-wide pelvic health integration to support veteran recovery