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Clinical Trials/NCT03717974
NCT03717974CompletedNot Applicable

Randomized Controlled Pilot Study for Medico-economic Impact Evaluation in Telemedecine Follow-up in Complement of a Mobile Team in Patients With Neurological Disabilities (HANDI@CCESS)

Pôle Saint Hélier2 sites in 1 country80 target enrollmentStarted: September 24, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
80
Locations
2
Primary Endpoint
Medical-economic analysis by the calculation of the cost-effectiveness of this organization of care

Study Overview

Brief Summary

Access to care for people with traumatic or degenerative neurological disabilities is a current public health concern. New technological tools such as telemedicine can bring expertise to the place of life of people while promoting the city-hospital link.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients over 18
  • Volunteer to participate in the study and whose primary caregiver is voluntary
  • Presenting a severe neurological handicap following a neurological lesion of traumatic, vascular or degenerative origin,
  • Requiring an expert opinion in MPR (rehabilitation, technical and human compensatory means, specific treatments ...) and / or in algology
  • Whose access to care is reduced (difficulties of movement, distance from expert centers, situation of fragility ...) and which necessitate the displacement of professionals at home,
  • Which require a coordination of care associating the professionals of the sanitary and medico-social sectors
  • Living in health territory 5 in Brittany
  • Mastering the French language spoken and / or written.

Exclusion Criteria

  • Misunderstanding making it impossible for informed consent with the refusal of the guardian or court safeguard
  • Unable to use a digital tablet or lack of a resource person who can assist the patient in the use of the tablet
  • Patients who do not have access to an internet connection (white area)
  • Life threatening is committed in the short term (< 3 months)

Outcomes

Primary Outcomes

Medical-economic analysis by the calculation of the cost-effectiveness of this organization of care

Time Frame: 6 months

Cost-effectiveness analysis by ICER (Incremental Cost-Effectiveness Ratio)

Secondary Outcomes

  • UTAUT (Unified theory of acceptance of technology) questionnaire(6 months)
  • DN4 scale(6 months)
  • Zarit's score(6 months)
  • EVA Satisfaction(6 months)
  • Hospital Anxiety and Depression scale (HAD)(6 months)
  • Doloplus scale(6 months)
  • Pain evaluation(6 months)
  • Goal Attainment Scale(6 months)

Investigators

Sponsor
Pôle Saint Hélier
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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