5 Day

Efforia Calendly Integration Test

STUDY TITLE Efforia Calendly Integration Test
Submitted under umbrella

Minimal Risk Citizen Science Umbrella Protocol

Date submitted

Jul 1, 2026

End date

There is no pre-specified end date and sub-studies remain open long-term.

Language

English

Efforia AI IRB approval recommendation

Recruitment page preview

Preview

Author edit

Edit

Informed consent

Review

Study author

Calendly Efforia, Zeeshan Web

Principal investigator

Matthew Amsden

Sub-Investigator for Adverse Events

Dr. Viral Patel

Description

Efforia Calendly Integration Test

Participant engagement length

5 Days

Sponsor

This study is made possible by your payment to cover all supplies and expenses required to participate.

Cost to participant

$0

Included products & services
30 Minute Meeting: $0
Outcome measures
Methodology

Single Arm longitudinal where participants act as their own control

Basic or advanced dissemination plan

Basic

Deviation from recruitment approach

No

Deviation from statistical approach

No

Will study include “more about you questions”

No

Clinicaltrials.Gov

Yes

Committment to list findings on clinicaltrials.Gov

Yes

This document is prepared with the assistance of AI, but is reviewed by a human.

Rational & Study Design

The Intervention

Efforia Calendly Integration aims to streamline appointment scheduling in clinical settings. Scientific evidence suggests such integrations enhance operational efficiency and patient satisfaction. The medical community acknowledges the potential for improved coordination and time management. Social media buzz highlights user-friendly interfaces and convenience, while the general population perceives it as beneficial for reducing wait times and improving access to care. Risks are minimal, primarily related to data privacy, with benefits including increased efficiency and patient engagement.

Included Products & Services

Product Name: 30 Minute Meeting

Quantity included: 0

Price: $0.00

Product Description: 30 Minute Meeting With Calendly

Product Image:

Ingredients:

Product Safety:

Study Design & Methodology

Inappropriate Participants & Inclusion/Exclusion

Study Design & Experience

Statistical Analysis Plan

Limitations & Justification

Human Subjects Ethics

Suitability Under Minimal Risk Umbrella Protocol

Suitability for Pay to Participate Model

Human Subjects Protection Questionnaire