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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06388694
Other study ID # RDO KPNC 24-056
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2, 2024
Est. completion date July 31, 2024

Study information

Verified date April 2024
Source Kaiser Permanente
Contact Tracy A Lieu, MD
Phone 5108913400
Email tracy.lieu@kp.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This cluster randomized trial will compare pharmacist management of secure message requests for refills of attention deficit hyperactivity medications with primary care physician management regarding quality of care, timeliness of service, and parent care experience.


Description:

Importance. Enhancing the management of messages from patients and providing high-quality, consistent care are top priorities for The Permanente Medical Group (TPMG) and Kaiser Foundation Hospitals/Health Plan (KFH/P). A special extension of the Ryan Haight Act currently enables providers to prescribe controlled substances via telehealth interactions, but expires in December 2024. Information about the quality of care provided via telehealth prescribing of controlled substances by pharmacists and primary care physicians would be helpful to inform care delivery within Kaiser Permanente and beyond. Objective. To compare pharmacist management of secure message requests for refills of attention deficit hyperactivity disorder (ADHD) medications with primary care physician management regarding quality of care, efficiency of service, and parent satisfaction. Design, setting, and participants. This cluster randomized clinical trial will include parents of children in Kaiser Permanente Northern California who request ADHD medication refills via secure messages from April 29 to June 28, 2024. Of KPNC's 63 facilities eligible for inclusion, we will assign 32 to Pharmacist Care and 31 to PCP Care. Intervention. In the intervention group, a regional team of pharmacists will manage ADHD medication refill requests made via secure message using a standard protocol. In the comparison group, primary care physicians (pediatricians and family medicine physicians) will manage these visits using a similar protocol. Main Outcomes and Measures. The primary outcome is whether a patient who did not have a weight recorded in the 6 months before the refill request was referred for a primary care follow-up visit. Secondary outcomes are the days from the secure message request to the prescription order and medication fill, and parent satisfaction. Potential Results. We will test the hypotheses that Pharmacist Care compared with PCP Care will have higher quality of care, faster time to prescriptions and fills, and higher patient satisfaction. Potential Conclusions and Relevance. If pharmacist care for ADHD medication refill requests has better or similar outcomes compared with PCP care, this will provide evidence supporting continuation of this approach. This study's findings will be useful for KPNC and to inform discussions about renewing the special extension of the Ryan Haight Act that allows this approach.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 315
Est. completion date July 31, 2024
Est. primary completion date June 28, 2024
Accepts healthy volunteers No
Gender All
Age group 2 Years to 17 Years
Eligibility Inclusion Criteria: - Parent or caregiver requested an ADHD medication refill via a secure message Exclusion Criteria: - The ADHD medication refill request was not straightforward and had to be handled by the primary care provider (and thus not eligible for random assignment to Pharmacist Care or PCP Care)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pharmacist Care
Pharmacists will provide ADHD medication refill orders in response to secure message requests by parents, under the authorization of appropriate physicians.
Primary Care Physician Care
Primary care pediatricians will provide ADHD medication refill orders in response to secure message requests by parents. This is usual care.

Locations

Country Name City State
United States Kaiser Permanente Northern California Oakland California

Sponsors (1)

Lead Sponsor Collaborator
Kaiser Permanente

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of participants appropriately referred for a follow-up weight check Percentage of participants referred for a follow-up visit for a weight check, among those who had not had a weight check in the 6 months prior to the medication refill request within 7 days after the refill request
Secondary Timeliness of care Days between the refill request and the refill order, among patients eligible for a refill within 14 days after the refill request
Secondary Parent perception of effectiveness of care Parent or caregiver perception of effectiveness of care given by the provider responding to the secure message request, as measured by a 5-point LIkert scale using Excellent, Very Good, Good, Fair, and Poor response options within 3 weeks after the refill request
See also
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Active, not recruiting NCT05286762 - Phase 3 Efficacy and Safety Fixed-Dose Study in Pediatrics (6-17) With ADHD Using CTx-1301 Phase 3
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