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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02030379
Other study ID # MCC-14970
Secondary ID HM14970
Status Terminated
Phase N/A
First received December 10, 2013
Last updated July 6, 2015
Start date July 2013
Est. completion date November 2014

Study information

Verified date July 2015
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The investigators will leverage e-technologies to provide an online version of the Question Prompt LIst (QPL-CT), that patients access via available iPads, enabling both the real-time prioritizing of patient questions as well as the seamless delivery of these questions to their treating physician (and other members of their clinical team) via the VCU Health System (VCUHS) patient portal, and the electronic medical record (EMR) prior to a consultation to discuss a clinical trial


Description:

The investigators propose to conduct pilot work to inform our knowledge of optimal methods of utilizing QPLs and will use the QPL-CT as an example. The investigators will leverage e-technologies to provide an online version of the QPL-CT, that patients access via available iPads, enabling both the real-time prioritizing of patient questions as well as the seamless delivery of these questions to their treating physician (and other members of their clinical team) via the VCU Health System (VCUHS) patient portal, and the EMR prior to a consultation to discuss a clinical trial. The investigators will use a pilot randomized clinical trial design to demonstrate the efficacy of the online QPL-CT versus a paper and pencil QPL-CT to increase question asking, patient understanding of trial information and reduce patients conflict over their upcoming decision to join a trial


Recruitment information / eligibility

Status Terminated
Enrollment 8
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Cancer diagnosis

- Fluent in English

- eligible for a therapeutic clinical trial

- Patients of recruited oncologists

Exclusion Criteria:

- Healthy subjects

- Not eligible for a therapeutic clinical trial

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
QPL-CT
Use the QPL-CT to prioritize questions

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (1)

Lead Sponsor Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Test the feasibility of using the online QPL-CT for patients and physicians Patients will complete an exit interview at the completion of patient's consultation asking about the patient's impressions of the online QPL-CT including its ease of use and the patient's perceptions of its influence on consultation communication. Physicians will complete a brief interview on one occasion at the completion of patient recruitment asking about the impact of the prioritized QPL-CT on consultation communication. 30 days No
Primary Online QPL-CT to Oncologist Use online QPL-CT to prioritize their questions and the prioritized list will be conveyed to their oncologist. Investigators will evaluate the efficacy of the online QPL-CT to increase question asking, patient understanding of trial information and reduce patients conflict over their upcoming decision to join a trial. 30 days No
Secondary Impact of providing physicians patient's QPL-CT Examine the impact of providing physicians their patient's prioritized QPL-CT on information provision and decision making process as measured by the Decision Analysis System for Oncology 30 days No
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