Comfort Talk and Economic Outcomes in MRI (ComfortTalk®)

August 6, 2019 updated by: Elvira V. Lang, MD, Hypnalgesics, LLC

Amelioration of Claustrophobia and Disruptive Patient Motion in MRI Imaging (Phase 2 Randomized Training of Sites)

Annually, an estimated 700,000 patients do not complete their scheduled MRI scans because of claustrophobia or inability to hold still. Training staffs working in MRI facilities to provide Comfort Talk® will enable patients to complete high quality imaging without medication, which will increase satisfaction and comfort while reducing sedation risks for patients, and increase efficiency and reduce loss of revenue for facilities. The effect of such training will be tested at 12 MRI sites in a randomized design. Outcome data will be collected for one year.

Study Overview

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

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Brookline, Massachusetts, United States, 02446
        • Hypnalgesics, LLC
    • North Carolina
      • Durham, North Carolina, United States, 27710
        • Duke University Medical Center
    • Ohio
      • Columbus, Ohio, United States, 43210
        • Ohio State University Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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.
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:
  • Self-hypnotic relaxation
  • Nonpharmacologic analgesia
  • Nonpharmacologic anxiolysis
  • Patient sedation without medication
No Intervention: Control
MRI sites not trained in Comfort Talk®.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Equipment Utilization Q4FY15 = Baseline Quarter (OSU)
Time Frame: 1 quarter
Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
1 quarter
Equipment Utilization in Q1FY16 (OSU)
Time Frame: 1 quarter
Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
1 quarter
Equipment Utilization in Q2FY16 (OSU)
Time Frame: 1 quarter
Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
1 quarter
Equipment Utilization in Q3FY16 (OSU)
Time Frame: 1 quarter
Quarterly completion rate of MRIs as a proportion of scans completed per given number of imaging slots available
1 quarter
Equipment Utilization Over All Quarters (OSU)
Time Frame: 4 quarters
Completion rates of MRIs as a proportion of scans completed per given number of imaging slots available
4 quarters
Incompletions (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Patients who cannot complete their scan
9 months (3 months baseline, 6 months post training)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
No-shows in Q4FY15 = Baseline Quarter (OSU)
Time Frame: 1 quarter
Quarterly number of scheduled patients who do not show up for their appointments
1 quarter
No-shows in Q1FY16 (OSU)
Time Frame: 1 quarter
Quarterly number of scheduled patients who do not show up for their appointments
1 quarter
No-shows in Q2FY16 (OSU)
Time Frame: 1 quarter
Quarterly number of scheduled patients who do not show up for their appointments
1 quarter
No-shows in Q3FY16 (OSU)
Time Frame: 1 quarter
Quarterly number of scheduled patients who do not show up for their appointments
1 quarter
Trend of No-shows Over All Quarters (OSU)
Time Frame: 4 quarters
Quarterly number of scheduled patients who do not show up for their appointments
4 quarters
Patient Satisfaction Ranking in Q4FY15 = Baseline Quarter (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.
1 quarter
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.
1 quarter
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.
1 quarter
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.
1 quarter
Oral Sedation Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Patients who receive medical sedation on site
9 months (3 months baseline, 6 months post training)
IV Sedation Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Number of patients who receive intravenous (IV) sedation on site
9 months (3 months baseline, 6 months post training)
General Anesthesia Rate (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Number of patients who receive general anesthesia on site
9 months (3 months baseline, 6 months post training)
Disruptive Motion (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Patients on site who disrupt the scan by motion
9 months (3 months baseline, 6 months post training)
No-shows (Duke)
Time Frame: 9 months (3 months baseline, 6 months post training)
Scheduled patients who do not show for their MRI examinations.
9 months (3 months baseline, 6 months post training)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2015

Primary Completion (Actual)

July 31, 2017

Study Completion (Actual)

July 31, 2017

Study Registration Dates

First Submitted

April 20, 2015

First Submitted That Met QC Criteria

April 27, 2015

First Posted (Estimate)

April 28, 2015

Study Record Updates

Last Update Posted (Actual)

September 12, 2019

Last Update Submitted That Met QC Criteria

August 6, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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