"Learning About Biologics"-Rheumatoid Arthritis
|ClinicalTrials.gov Identifier: NCT01721200|
Recruitment Status : Completed
First Posted : November 5, 2012
Results First Posted : February 19, 2018
Last Update Posted : February 19, 2018
|Condition or disease||Intervention/treatment|
|Rheumatoid Arthritis||Other: Decision Support Tool Other: Usual Care|
Data suggest that undertreatment of rheumatoid arthritis (RA) patients may be in part due to inadequate decision support when they face whether or not to start biologic therapy. No proven way exists to inform or support RA patients who are candidates for biologic therapy. Communicating information about biologic medication is particularly challenging because of the sheer number of risks to disclose, the difficulty explaining the risks of extremely rare adverse events (AEs), and the tendency for people to discount (or underweight) future benefits.
Dr Liana Fraenkel at Yale University is the Primary Investigator and developer of this theory-based high quality decision support tool to effectively inform RA patients who are candidates for biologics. Dr. Eric Newman will be Principal Investigator for the project which will be conducted at Geisinger Medical Center. All subjects enrolled will complete a baseline survey and then will be randomized to use of the decision support tool or to usual care. Those randomized to usual care will be offered the opportunity to access the tool once enrollment is closed and all follow-up visits have been completed.
Outcomes will be assessed at two and six weeks after the baseline visit by the Geisinger Telephone Survey and Interviewing Facility. This facility is equipped with 12 computers and runs two shifts a day. The Survey Unit uses a state-of-the-art Windows based Computer Assisted Telephone Interview (CATI) system to administer surveys and collect research data. The group holds 12 interviewer licenses for the CATI system. Trained and experienced interviewers are available to make the calls from 9 am to 9 pm Monday through Friday and from 10 am to 2 pm on Saturdays.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||125 participants|
|Intervention Model:||Parallel Assignment|
|Primary Purpose:||Supportive Care|
|Official Title:||"Learning About Biologics"|
|Study Start Date :||November 2012|
|Primary Completion Date :||February 2015|
|Study Completion Date :||February 2015|
Decision Support Tool
This study will examine the efficacy of a web-based educational decision support tool.
Other: Decision Support Tool
Educational decision support tool for patients with rheumatoid arthritis
Usual Care Group will receive their biologic drug teaching from their rheumatologist.
Other: Usual Care
Subjects randomized to the Usual Care Group will receive their biologic drug teaching from the rheumatologist as part of their routine care.
- The Proportion of Subjects Who Are Classified as Having Made an Informed Value Concordant Choice at 2 Weeks [ Time Frame: 2 weeks ]We classified subjects as having made an informed choice to escalate care if they answered at least 75% of the knowledge questions correctly and had low decisional conflict as defined by a score of 25 or lower on the combined subjective knowledge and values clarity subscales.
- Patient-physician Communication [ Time Frame: 8 weeks ]Patient-physician communication will be measured using the COMRADE (Combined Outcome Measure for Risk communication And treatment Decision making Effectiveness): a 20-item scale composed of two subscales which address the quality of risk communication (process measure) and the quality of the decision making process (outcome measure). Items are measured on a 5-point agree scales. The COMRADE is a includes two sub-scales (each composed of 10 items): one for risk communication (a process measure) and a second for confidence in decision (an outcome measure). Subscales are summed to generate a total score (Range 20-100). Higher scores reflect poorer outcomes.
- Use of Biologics [ Time Frame: 8 weeks ]Use of biologics: The number of patients received a prescription for a new biologic by eight weeks.
- To Test Screening and Recruitment Procedures [ Time Frame: 8 weeks ]To test screening and recruitment procedures we will measure the number of eligible patients, the number of patients excluded by each exclusion criterion, the number of patients referred by rheumatologists each week, and the proportion of patients who agree to participate.
- To Test Uptake [ Time Frame: 8 weeks ]To test uptake and adherence to the intervention we will measure the proportion of patients randomized to the intervention who access the tool, complete the Best Worse Scaling exercise, print a handout, and use the handout during a follow-up visit with their rheumatologist (for subjects having a second visit within eight weeks). Note, subjects without access to a printer will have the opportunity to do so in the office.
- Acceptability to Physicians [ Time Frame: 8 weeks ]
Acceptability to physicians will be assessed using four items coded on 5-point Frequency scales (1= None of the time and 5= All of the time) administered by the research assistant once all patient follow-up interviews have been completed:
- Did the tool make it easier to talk about treatment with your patients?
- Did the tool increase the amount of time you spent discussing therapy with your patients?
- Did the tool decrease the amount of time you spent discussing therapy with your patients?
- Did the tool improve the quality of informed consent for patients initiating biologics?
- To Test Adherence to the Intervention [ Time Frame: 8 weeks ]The session management system will record the time spent on each module visited within the tool to assess adherence.
- Changes in Knowledge [ Time Frame: 8 weeks ]Knowledge will be measured using the 20 True/False statements developed for the initial pre-post test study. The number of correct responses are summed to yield a knowledge score (possible range= 0-20). The item order was determined using a random-numbers generator.
- Changes in Willingness [ Time Frame: 8 weeks ]Willingness: Patients' propensity towards biologics will be measured using the choice predisposition scale (65): This item is coded on a 11-point scale anchored by "Not willing at all" and "Extremely willing" with "Unsure" at the midpoint (65). Higher scores reflect greater willingness.
- Changes in Perceived Knowledge [ Time Frame: 8 weeks ]Perceived knowledge and value clarity will be measured using two subscales from the well-validated Decisional Conflict Scale (66). Each subscale is composed of 3 items measured on 5-point agree scales. Scores are rescaled to range from 0 to 100. Higher scores reflect greater conflict (poorer outcomes).
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01721200
|United States, Pennsylvania|
|Geisinger Medical Center|
|Danville, Pennsylvania, United States, 17822|
|Principal Investigator:||Liana Fraenkel, MD, MPH||Yale University|