- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02427737
Comfort Talk and Economic Outcomes in MRI (ComfortTalk®)
Amelioration of Claustrophobia and Disruptive Patient Motion in MRI Imaging (Phase 2 Randomized Training of Sites)
Study Overview
Status
Intervention / Treatment
Detailed Description
Claustrophobia and disruptive patient motion are common impediments to MRI examination, but they may be prevented or ameliorated with a non-pharmacologic behavioral intervention administered by trained staff. The potential benefits of such an intervention are highly significant, considering that the alternatives are to cancel the study or administer sedation. Inability to complete their MRI scans adversely affects an estimated 700,000 patients every year in the US. These patients are either deprived of a diagnosis, subject to diagnostic delays and interpretation errors due to motion artifact, or are exposed to risks of pharmacologic sedation, including death. The imaging facilities typically cannot fill the suddenly vacated examination slots in time before the next scheduled patient and incur considerable lost revenue and efficiency. A negative patient experience further jeopardizes Value-Based reimbursement by the Centers for Medicare and Medicaid Services (CMS) towards which patient satisfaction counts 30%. The long term goal is to provide a validated, clinically feasible means for non-pharmacologic amelioration of claustrophobia and disruptive patient motion, achieved by training facility staff in Comfort Talk®.
Comfort Talk® training consists of a proprietary, standardized R3 Process of Rapport, Relaxation, and Reframing including 2 x 8-hrs class-room interaction, onsite coaching, and institution-specific web-based support to help the MRI team to further develop its own language style and skill set.
The effect of Comfort Talk® training will be quantified in a prospective randomized design at 12 MRI satellites of the Ohio State University Medical Center and Duke University Medical Center. Return of investment of training will be based on a decision-analysis model with focus on number of scans performed, cancellations from no-shows and refusals; patients unable to start or complete a scan; and sedation rates in relation to capacity, cost, and reimbursement schedule. Patient satisfaction scores will be compared using Press Ganey national benchmark percentile rankings and CMS quality standards.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Massachusetts
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Brookline, Massachusetts, United States, 02446
- Hypnalgesics, LLC
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North Carolina
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Durham, North Carolina, United States, 27710
- Duke University Medical Center
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Ohio
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Columbus, Ohio, United States, 43210
- Ohio State University Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Must routinely perform MRI examinations
- Must capture data on noncompletion of MRI scans
Exclusion Criteria:
- No dedicated MRI unit
- Unable to reliably capture data on noncompletion of MRI scans
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Comfort Talk® Training
In the experimental group, MRI personnel is trained to use Comfort Talk® to help patients who are claustrophobic, anxious, and/or cannot lie still to complete their tests at the onset of the MRI scan.
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Personnel of MRI units is trained in advanced rapport skills, patient-centered and hypnoidal language, correct use of suggestions and skills of tension diffusion.
This entails 16 hrs classroom work, additional on-site post-training support, and access to a post-training support web module resulting in at least 20 hrs training.
Other Names:
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No Intervention: Control
MRI sites not trained in Comfort Talk®.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Equipment Utilization Q4FY15 = Baseline Quarter (OSU)
Time Frame: 1 quarter
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Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
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1 quarter
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Equipment Utilization in Q1FY16 (OSU)
Time Frame: 1 quarter
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Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
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1 quarter
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Equipment Utilization in Q2FY16 (OSU)
Time Frame: 1 quarter
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Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
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1 quarter
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Equipment Utilization in Q3FY16 (OSU)
Time Frame: 1 quarter
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Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
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1 quarter
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Equipment Utilization Over All Quarters (OSU)
Time Frame: 4 quarters
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Completion rates of MRIs as a proportion of scans completed per given number of imaging slots available
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4 quarters
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Incompletions (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Patients who cannot complete their scan
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9 months (3 months baseline, 6 months post training)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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No-shows in Q4FY15 = Baseline Quarter (OSU)
Time Frame: 1 quarter
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Quarterly number of scheduled patients who do not show up for their appointments
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1 quarter
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No-shows in Q1FY16 (OSU)
Time Frame: 1 quarter
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Quarterly number of scheduled patients who do not show up for their appointments
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1 quarter
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No-shows in Q2FY16 (OSU)
Time Frame: 1 quarter
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Quarterly number of scheduled patients who do not show up for their appointments
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1 quarter
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No-shows in Q3FY16 (OSU)
Time Frame: 1 quarter
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Quarterly number of scheduled patients who do not show up for their appointments
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1 quarter
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Trend of No-shows Over All Quarters (OSU)
Time Frame: 4 quarters
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Quarterly number of scheduled patients who do not show up for their appointments
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4 quarters
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Patient Satisfaction Ranking in Q4FY15 = Baseline Quarter (OSU)
Time Frame: 1 quarter
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Quarterly percentile rankings of patients' "Overall Assesment" of their satisfaction on a national clinical survey instrument (Press Ganey).
Percentile rankings are benchmarked on 1,028 MRI sites nationally, given in raw scores between 0 (worst) to 100 (best).
The percentile rankings are based on the number of participants returning surveys in each group.
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1 quarter
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Patient Satisfaction in Q1FY16 (OSU)
Time Frame: 1 quarter
|
Quarterly percentile rankings of patients' "Overall Assesment" of their satisfaction on a national clinical survey instrument (Press Ganey).
Percentile rankings are benchmarked on 1,028 MRI sites nationally, given in raw scores between 0 (worst) to 100 (best).
The percentile rankings are based on the number of participants returning surveys in each group.
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1 quarter
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Patient Satisfaction Ranking in Q2FY16 (OSU)
Time Frame: 1 quarter
|
Quarterly percentile rankings of patients' "Overall Assesment" of their satisfaction on a national clinical survey instrument (Press Ganey).
Percentile rankings are benchmarked on 1,028 MRI sites nationally, given in raw scores between 0 (worst) to 100 (best).
The percentile rankings are based on the number of participants returning surveys in each group.
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1 quarter
|
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Patient Satisfaction Ranking in Q3FY16 (OSU)
Time Frame: 1 quarter
|
Quarterly percentile rankings of patients' "Overall Assesment" of their satisfaction on a national clinical survey instrument (Press Ganey).
Percentile rankings are benchmarked on 1,028 MRI sites nationally, given in raw scores between 0 (worst) to 100 (best).
The percentile rankings are based on the number of participants returning surveys in each group.
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1 quarter
|
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Oral Sedation Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Patients who receive medical sedation on site
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9 months (3 months baseline, 6 months post training)
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IV Sedation Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Number of patients who receive intravenous (IV) sedation on site
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9 months (3 months baseline, 6 months post training)
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General Anesthesia Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Number of patients who receive general anesthesia on site
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9 months (3 months baseline, 6 months post training)
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Disruptive Motion (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Patients on site who disrupt the scan by motion
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9 months (3 months baseline, 6 months post training)
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No-shows (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
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Scheduled patients who do not show for their MRI examinations.
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9 months (3 months baseline, 6 months post training)
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Lang EV, Benotsch EG, Fick LJ, Lutgendorf S, Berbaum ML, Berbaum KS, Logan H, Spiegel D. Adjunctive non-pharmacological analgesia for invasive medical procedures: a randomised trial. Lancet. 2000 Apr 29;355(9214):1486-90. doi: 10.1016/S0140-6736(00)02162-0.
- Lang EV, Rosen MP. Cost analysis of adjunct hypnosis with sedation during outpatient interventional radiologic procedures. Radiology. 2002 Feb;222(2):375-82. doi: 10.1148/radiol.2222010528.
- Lang EV, Yuh WT, Ajam A, Kelly R, Macadam L, Potts R, Mayr NA. Understanding patient satisfaction ratings for radiology services. AJR Am J Roentgenol. 2013 Dec;201(6):1190-5; quiz 1196. doi: 10.2214/AJR.13.11281.
- Norbash A, Yucel K, Yuh W, Doros G, Ajam A, Lang E, Pauker S, Mayr N. Effect of team training on improving MRI study completion rates and no-show rates. J Magn Reson Imaging. 2016 Oct;44(4):1040-7. doi: 10.1002/jmri.25219. Epub 2016 Apr 6.
- Lang EV, Ward C, Laser E. Effect of team training on patients' ability to complete MRI examinations. Acad Radiol. 2010 Jan;17(1):18-23. doi: 10.1016/j.acra.2009.07.002. Epub 2009 Sep 5.
- Lang EV. A Better Patient Experience Through Better Communication. J Radiol Nurs. 2012 Dec 1;31(4):114-119. doi: 10.1016/j.jradnu.2012.08.001.
- Flory N, Lang EV. Distress in the radiology waiting room. Radiology. 2011 Jul;260(1):166-73. doi: 10.1148/radiol.11102211. Epub 2011 Apr 7.
- Lang EV, Hatsiopoulou O, Koch T, Berbaum K, Lutgendorf S, Kettenmann E, Logan H, Kaptchuk TJ. Can words hurt? Patient-provider interactions during invasive procedures. Pain. 2005 Mar;114(1-2):303-9. doi: 10.1016/j.pain.2004.12.028. Epub 2005 Jan 26.
- Ajam AA, Nguyen XV, Kelly RA, Ladapo JA, Lang EV. Effects of Interpersonal Skills Training on MRI Operations in a Saturated Market: A Randomized Trial. J Am Coll Radiol. 2017 Jul;14(7):963-970. doi: 10.1016/j.jacr.2017.03.015. Epub 2017 Apr 28.
- Ladapo JA, Spritzer CE, Nguyen XV, Pool J, Lang E. Economics of MRI Operations After Implementation of Interpersonal Skills Training. J Am Coll Radiol. 2018 Dec;15(12):1775-1783. doi: 10.1016/j.jacr.2018.01.017. Epub 2018 Mar 9.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2CTOSUD2015
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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