- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01283633
Investigation of the Use of Remote Presence Robots in Delivery of Neuromodulation
Investigation of the Use of Remote Presence Robots in the Administration of Neuromodulation Treatment
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Patients with neuromodulation systems implanted for either movement disorders or chronic pain and who require programming of their systems will be approached to enter the study. Those who consent will be consecutively assigned to either the normal standard of care (i.e. programming of their systems with an experienced clinician) or programming of their systems with an inexperienced programmer (nurse) who will be directed by the experienced programmer via the remote presence robot. Both the nurses and the patients will complete questionnaires rating their satisfaction of the programming experience.
They will each only receive one questionnaire at the end of the programming session. There is no other test point.
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 4
Kontakter och platser
Studieorter
-
-
Nova Scotia
-
Halifax, Nova Scotia, Kanada, B3H 1V7
- Centre for Clinical Research, Queen Elizabeth II Health Sciences Centre
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- patients with neuromodulation systems, requiring programming
- nurses who have never programmed a neuromodulation system before
Exclusion Criteria:
- those who are unwilling to give consent
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: programming with non-experienced nurse
Programming done by an experienced neuromodulation clinician will be compared to the patient satisfaction of a programming session with an inexperienced nurse via remote presence robotics, which will be directed by the experienced clinician
|
Neuromodulation as directed via remote presence robotic and experienced clinician for those with neuromodulation systems implanted to treat movement disorders and chronic pain
Andra namn:
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Patient Satisfaction
Tidsram: Patients will complete the questionnaire once following the neuromodulation therapy. Day 1
|
The questionnaire will take approximately 10 minutes to complete.
There are no other follow-ups required.
This is the only study time commitment for the patients above the usual standard of care.
|
Patients will complete the questionnaire once following the neuromodulation therapy. Day 1
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Nursing satisfaction questionnaire
Tidsram: Immediately following the neuromodulation session, the nurse will complete one questionnnaire. Day 1.
|
The questionnaire will take approximately 10 minutes to complete.
The time commitment from the nurse programmer will be approximately 45 minutes.
There are no other test points nor follow up visits.
|
Immediately following the neuromodulation session, the nurse will complete one questionnnaire. Day 1.
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Ivar M Mendez, MD, Capital Health and Dalhousie University
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- Robotics-Neuromod-Mendez
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