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NCT02309905 Clinical Trial

Evaluation of Tele-expertise for Inmates With a Dermatological Lesion

Skin Disease Clinical Trial

— TLM-Inmates  

Official title:
Evaluation of Tele-expertise for Inmates With a Dermatological Lesion

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02309905
Other study ID # Teledermatology for Inmates
Secondary ID
Status Completed
Phase N/A
First received November 27, 2014
Last updated January 14, 2016
Start date June 2014
Est. completion date December 2015

Study information
Verified date December 2015
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether Tele-expertise would be effective and cost-effective by reducing the number of secure transportations for inmates in need of a dermatological consultation

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date December 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Dermatological expertise required

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Device:
• Telemedicine
Inmates of prisons having telemedicine after implementation of telemedicine

Locations
Country Name City State
France UCSA Osny Cergy-Pontoise
France UCSA Meaux Meaux
France UCSA Nanterre Nanterre
France UCSA Réau Réau
France UCSA Villepinte Villepinte

Sponsors (2)
Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris Agence Regionale de Sante d'Ile de France

Country where clinical trial is conducted

France, 

References & Publications (1)

Kidholm K, Ekeland AG, Jensen LK, Rasmussen J, Pedersen CD, Bowes A, Flottorp SA, Bech M. A model for assessment of telemedicine applications: mast. Int J Technol Assess Health Care. 2012 Jan;28(1):44-51. doi: 10.1017/S0266462311000638. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Proportion of a dermatological expertise among those required 1 month after the end of the study No
Secondary Number of hospitalizations for a dermatological reason 1 month after the end of the study Yes
Secondary Overall costs 6 months after the end of the study No
Secondary Time to a dermatological expertise 1 month after the end of the study No
Secondary Number of usual consultations needed after Tele-expertise 1 month after the end of the study Yes
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