- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00488293
Impact of Teledermatology on Health Services Outcomes in the Department of Veterans Affairs
Impact of Teledermatology on Health Services Outcomes in the VA
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Anticipated Impact on Veterans' Healthcare - Teledermatology has the potential to have a significant impact on veterans' healthcare. There is an unmet demand for Dermatology services distributed throughout a nation-wide patient base. Decentralization of care through the expansion of Community Based Outpatient Centers (CBOCs) adds to the demand for these services. Dermatologic care typically resides only at the largest medical centers within a Veterans Integrated Service Network (VISN). Teledermatology is one means of meeting the demand for Dermatology services by delivering dermatologic care to those sites that are geographically removed from the Dermatology Consult Service.
Project Background - For the majority of ambulatory skin conditions encountered in Primary Care and Dermatology Clinics the impact those conditions have on patients' quality of life is of principal importance. Commonly encountered skin diseases frequently result in discomfort or pain, pruritis, emotional concerns, embarrassment, anxiety, and interfere with activities of daily living, work activities, or interpersonal relations. To date, no data exist that compares quality of life outcomes - the fundamental metric to assess in an ambulatory dermatology population - between patients undergoing store and forward teledermatology consultations with patients managed by the conventional consult processes. Existing data does indicate that teledermatology is a reliable and accurate method of diagnosing skin disease.
Research Objectives - The purpose of this study was to compare store and forward teledermatology with a conventional clinic-based dermatology consultation process. Our primary objective was to determine whether the mean change in patient quality of life, as rated by the composite score and subscale scores of a skin-specific quality of life index (Skindex-16), differed between the time of randomization and 9 months for patients evaluated by store and forward teledermatology compared to conventional consult methods. Secondary objectives included (a) assessing quality of life between time of randomization and 3 months, (b) assessing time to initial definitive evaluation for patients using each modality, (c) evaluating clinical course using serial digital imaging, (d) comparing the costs and cost-effectiveness of store and forward teledermatology with conventional consult methods.
Project Methods - The study was a parallel-group, superiority, randomized clinical trial that compared store and forward teledermatology with a conventional clinic-based consult process. Patients were randomized using a simple randomization scheme stratified by site to one of the two consult modalities. Eligible patients included those being referred from the remote sites of primary care to the medical center-based sites of dermatology services. Skindex-16 was administered at baseline, 3 months, and 9 months. Time to initial definitive evaluation, calculated based on the need for and timing of a clinic-based visit was measured for both groups. Using digital images, clinical course was assessed on a 5 point scale by an expert panel of three dermatologists. Categories included resolved, improved, unchanged not clinically relevant, unchanged clinically relevant, and worse. Health care utilities were measured using time trade-off data and the Health Utilities Index Mark 2 (HUI2). We compared the costs of teledermatology with conventional consult methods by estimating the average cost per patient over the 9 month study period. Effectiveness was assessed using health care utilities and time to initial definitive evaluation. Costs were estimated from the VA perspective.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
-
Minneapolis, Minnesota, United States, 55417
- Minneapolis VA Health Care System, Minneapolis, MN
-
-
Missouri
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Columbia, Missouri, United States, 65201-5297
- Harry S. Truman Memorial, Columbia, MO
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with a single non-emergent skin condition being referred to a VA Dermatology Clinic
- Must be a veteran at the study site
Exclusion Criteria:
- Full body examination requested
- Unable to read or speak English
- Emergent skin condition
- Pending dermatology appointment within 9 months
- Previous enrollment in the study
- Impending move from the area
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arm 1
Store and forward teledermatology consult process
|
Standard electronic consult, standardized history, and image set
Other Names:
|
|
No Intervention: Arm 2
Conventional consult process
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skindex-16 Change Scores Between Baseline to Month 9 - Composite Score
Time Frame: Baseline to Month 9
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 9
|
|
Skindex-16 Change Scores Baseline to Month 3 - Composite Score
Time Frame: Baseline to Month 3
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 3
|
|
Skindex-16 Change Scores Baseline to Month 9 - Symptoms Score
Time Frame: Baseline to Month 9
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 9
|
|
Skindex-16 Changes Scores Baseline to Month 3 - Symptoms Score
Time Frame: Baseline to Month 3
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 3
|
|
Skindex-16 Change Scores Between Baseline and Month 9 - Emotions Score
Time Frame: Baseline to Month 9
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 9
|
|
Skindex-16 Change Scores Between Baseline to Month 3 - Emotions Score
Time Frame: Baseline to Month 3
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 3
|
|
Skindex-16 Change Scores Between Baseline and Month 9 - Functioning Scores
Time Frame: Baseline to Month 9
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 9
|
|
Skindex-16 Change Scores Between Baseline and Month 3 - Functioning Score
Time Frame: Baseline to Month 3
|
Skindex-16 Change Scores.
Skindex-16 is a quality of life measure that assesses "bother."
It includes the domains of symptoms, emotions, and functioning.
A composite (total) score can also be calculated.
The range of scores are 0 (never bothered) to 100 (always bothered) for subscale and composite scores.
A negative change score represents a better quality of life.
A change score of 10 points is considered clinically significant.
|
Baseline to Month 3
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical Course Rating Between Baseline and Month 9
Time Frame: Baseline to Month 9
|
Clinical course was assessed by review of serial digital images.
The clinical course rating was provided by consensus opinion provided by a panel of three dermatologists that were not otherwise involved in the study.
The rating categories were resolved, improved, unchanged - not clinically relevant, unchanged - clinically relevant, and worse.
|
Baseline to Month 9
|
|
Clinical Course Rating Between Baseline and First Clinic Visit
Time Frame: Baseline to First Clinic Visit
|
Clinical course was assessed by review of serial digital images.
The clinical course rating was provided by consensus opinion provided by a panel of three dermatologists that were not otherwise involved in the study.
The rating categories were resolved, improved, unchanged - not clinically relevant, unchanged - clinically relevant, and worse.
|
Baseline to First Clinic Visit
|
Collaborators and Investigators
Investigators
- Principal Investigator: John D. Whited, MD MHS, Harry S. Truman Memorial, Columbia, MO
Publications and helpful links
General Publications
- Warshaw EM. The impact of store and forward teledermatology on quality of life: a randomized trial. Archives of dermatology. 2012 Jul 20.
- Whited JD, Warshaw EM, Kapur K, Edison KE, Thottapurathu L, Raju S, Cook B, Engasser H, Pullen S, Moritz TE, Datta SK, Marty L, Foman NA, Suwattee P, Ward DS, Reda DJ. Clinical course outcomes for store and forward teledermatology versus conventional consultation: a randomized trial. J Telemed Telecare. 2013 Jun;19(4):197-204. doi: 10.1177/1357633x13487116. Epub 2013 May 23.
- Whited JD, Warshaw EM, Edison KE, Kapur K, Thottapurathu L, Raju S, Cook B, Engasser H, Pullen S, Parks P, Sindowski T, Motyka D, Brown R, Moritz TE, Datta SK, Chren MM, Marty L, Reda DJ. Effect of store and forward teledermatology on quality of life: a randomized controlled trial. JAMA Dermatol. 2013 May;149(5):584-91. doi: 10.1001/2013.jamadermatol.380.
- Datta SK, Warshaw EM, Edison KE, Kapur K, Thottapurathu L, Moritz TE, Reda DJ, Whited JD. Cost and Utility Analysis of a Store-and-Forward Teledermatology Referral System: A Randomized Clinical Trial. JAMA Dermatol. 2015 Dec 1;151(12):1323-1329. doi: 10.1001/jamadermatol.2015.2362.
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIR 05-278
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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