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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03717974
Other study ID # 2017-A02378-45
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 24, 2018
Est. completion date January 25, 2022

Study information

Verified date February 2021
Source Pôle Saint Hélier
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date January 25, 2022
Est. primary completion date November 22, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Telemedecine follow-up after an intervention at home of the mobile team
After a first visit of the mobile team at home, patients are followed by telemedicine. Moreover, in case of pain, a specialized consultation by an algologist of "La Sagesse" will be realized.
Mobile team follow-up after an intervention at home of the mobile team
After a first visit of the mobile team at home, patients are followed by mobile team. Moreover, in case of pain, a specialized consultation by an algologist of "La Sagesse" will be realized.

Locations

Country Name City State
France Pôle Saint-Hélier Rennes

Sponsors (2)

Lead Sponsor Collaborator
Pôle Saint Hélier Clinique Mutualiste La Sagesse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Medical-economic analysis by the calculation of the cost-effectiveness of this organization of care Cost-effectiveness analysis by ICER (Incremental Cost-Effectiveness Ratio) 6 months
Secondary UTAUT (Unified theory of acceptance of technology) questionnaire Questionnaire of acceptability / acceptance of the tool and its use by professionals based on the Unified Theory of Acceptance and Use Technology (UTAUT) 6 months
Secondary Hospital Anxiety and Depression scale (HAD) It can detect anxiety and depressive disorders. It has 14 items rated from 0 to 3. Seven questions relate to anxiety (total A) and seven others to the depressive dimension (total D), thus obtaining two scores (maximum score of each score = 21). 7 or less: no symptomatology 8 to 10: doubtful symptomatology 11 and above: certain symptomatology. 6 months
Secondary Pain evaluation Digital assessment (0 to 10) of pain for communicating patients 6 months
Secondary DN4 scale Digital assessment of neuropathic pain for communicating patients. If the patient score is equal to or greater than 4/10, the test is positive. 6 months
Secondary Doloplus scale Behavioral Assessment Scale of Pain in Older People with Verbal Communication Disorders. This scale comprises ten items divided into three subgroups (five somatic, two psychomotor and three psychosocial).
Each item is rated from 0 to 3 (four exclusive and progressive level scoring), which results in an overall score between 0 and 30.
The pain is clearly affirmed for a score greater than or equal to 5 out of 30.
6 months
Secondary Zarit's score The Zarit scale assesses the emotional, physical and financial burden for caregivers of caring for someone with a loss of autonomy.
The total score, which is the sum of the scores obtained for each of 22 items, varies from 0 to 88.
A score less than or equal to 20 indicates a low or no load; a score between 21 and 40 indicates a light load; a score between 41 and 60 indicates a moderate load; a score above 60 indicates a severe charge.
6 months
Secondary Goal Attainment Scale Goal Attainment Scale by objectives at the beginning and end of taking charge. Each item built has 5 levels of answers 0: corresponds to the achievement of the goal set by the examiner.
1: is a better score than expected.
2: corresponds to the most favorable evolution expected.
1: corresponds to a score lower than that expected.
2: corresponds to a least favorable score expected.
6 months
Secondary EVA Satisfaction Digital assessment (0 to 10) of satisfaction. 6 months