Patient Navigation to Improve Surgical Access in Primary Hyperparathyroidism
- Conditions
- Hyperparathyroidism, Primary
- Interventions
- Other: Without Scheduling NavigationOther: Scheduling Navigation
- Registration Number
- NCT06562881
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
The goal of this study is to address surgical health equity in historically marginalized participants with primary hyperparathyroidism (PHPT). The main questions that this study aims to answer are, how does patient navigation impact:
* The proportion of PHPT participants undergo parathyroidectomy?
* The proportion of PHPT participants who complete surgical consultation?
* Time to surgical consultation?
* Time to surgery?
- Detailed Description
Patients historically marginalized in Medicine are at increased risk of delayed care and undertreatment of PHPT, which can result in end-organ damage and reduced quality of life due to fatigue, brain fog, pain and other constitutional symptoms due to imbalances in calcium levels. It can be easily treated with a highly curative, cost-effective, and low risk surgery but less than 40% of patients who qualify for surgery undergo treatment. Patients from historically marginalized populations such as black/Hispanic/Asian race, underinsurance, and older age are disproportionately impacted by lower rates of surgery and longer delays to surgery.
This pragmatic pilot trial aims to address surgical health equity in historically marginalized patients with PHPT by assessing the impact of navigation, specifically direct outreach and appointment scheduling, on conversion of surgical referral to consultation and conversion of surgical consultation to treatment in two dimensions, timeliness and clinical outcomes. Participants will be randomized to receive or not receive scheduling navigation at time of recruitment with a crossover design at 3 months for those who do not receive scheduling navigation at time of recruitment and have yet to complete surgical consultation.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 76
- Diagnosed with PHPT and not yet had parathyroidectomy who meet criteria for surgical treatment of PHPT (osteoporosis, fragility fracture, or evidence of vertebral compression fracture on spine imaging, renal involvement [renal stone, silent nephrolithiasis on renal imaging, nephrocalcinosis, hypercalciuria (24-hour urine calcium level 400 mg/dL) with increased stone risk, or impaired renal function (glomerular filtration rate 60 mL/min)], calcium 1 mg/dL above upper limit of normal, age less than 50)
- Qualify as a member of a racial or ethnic minority group (Black, Hispanic, Asian and Pacific Islander, Native American), lower socioeconomic neighborhoods (by zipcode), socially vulnerable (social determinants of health indicating financial strain, social vulnerability index in the top quartile 75%+ by zip code), or with underinsurance (Medicaid, Medicare, dual eligible, uninsured)
- Prior Parathyroidectomy
- End-stage Renal Disease
- Renal Transplant
- Vitamin D Deficiency
- Metastatic Disease
- Familial Hypocalciuric Hypercalcemia
- No Indication for Surgery
- Unable/Unwilling to provide consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Without Scheduling Navigation Without Scheduling Navigation Participants will not be assigned to a scheduler. Scheduling Navigation Scheduling Navigation Participants will be assigned to a scheduler.
- Primary Outcome Measures
Name Time Method Parathyroidectomy Surgical Outcome Within 12 months The primary outcome will be the proportion of patients who undergo parathyroidectomy
- Secondary Outcome Measures
Name Time Method Parathyroidectomy complications Assessed at 6 and 12 months after recruitment or surgery in all groups Complications rates of the following:
Bleeding/hematoma Hypocalcemia Surgical site infection Voice dysfunction TracheostomyCompletion of Consultation Through study completion, an average of 1 year after time of recruitment or surgery Proportion of participants who complete surgical consultation
Time to Consultation Through study completion, an average of 1 year after time of recruitment or surgery Time from participant referral to scheduling and completion of surgical consultation consultation
Time to Surgery Through study completion, an average of 1 year after time of recruitment or surgery Time from participant referral to surgery
Complications related to hyperparathyroidism Assessed at 6 and 12 months after recruitment or surgery in all groups New, worsening, or recurrent end organ disease (osteoporosis, kidney stone, renal impairment, mental health disorders or cognitive function (requiring hospitalization or loss of independence), pancreatitis)
Persistent hyperparathyroidism Assessed at 6 and 12 months after recruitment or surgery in all groups Rate of persistent disease, based on pattern of calcium and parathyroid hormone levels postoperatively
Recurrent hyperparathyroidism Assessed at 6 and 12 months after recruitment or surgery in all groups Rate of recurrent disease, based on pattern of calcium and parathyroid hormone levels postoperatively)
Surgical parathyroid re-exploration Assessed at 6 and 12 months after recruitment or surgery in all groups Rate of re-exploration for hyperparathyroidism
Trial Locations
- Locations (1)
Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States