Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neurotoxin Injections

Completed

• Conditions: Cervical Dystonia; Telemedicine
• Interventions: Other: Telemedicine follow-up visit

• Registration Number: NCT03969537
• Lead Sponsor: Vanderbilt University Medical Center

Brief Summary

Many cervical dystonia (CD) patients are limited in their ability to travel to the clinic for follow-up in between injection visits.

A telemedicine visit at the time of peak effectiveness of neurotoxin treatment may be valuable in informing the neurologist's choice of muscle selection and/or dose for the next injection visit. The primary objective of this study is to investigate both patient and physician satisfaction with the use of our telemedicine tool for this type of follow-up. After assessment of the subject, the neurologist will decide whether or not the telemedicine visit was informative to the upcoming injection visit. Subjects will answer questions at the end of the visit regarding their satisfaction with the follow-up and overall telemedicine communication. The principle investigator will complete a similar survey with additional questions about information gathered from the visit to assess the primary objective.

A secure video communications platform will be used for the visit, which will occur 2-4 weeks after the patient's last neurotoxin injection (around the time of peak effectiveness). The investigating neurologist will remotely assess the patient and make notes for the next injection visit.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2019-04-01
• Study First Submitted: 2019-05-29
• Study First Submitted QC: 2019-05-29
• Study First Posted: 2019-05-31
• Primary Completion: 2020-06-04
• Study Completion: 2020-06-04
• Status Verified: 2020-10
• Last Update Submitted: 2020-10-30
• Last Update Posted: 2020-11-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 27

Inclusion Criteria

• Male or female subjects of any race, aged 18 and above
• Diagnosed with cervical dystonia and being treated with neurotoxin injections at Vanderbilt University Medical Center
• The subject, or if appropriate their medical decision maker, is willing and able to provide written informed consent.
• Email and internet access
• Personal computing device with audio/video capability

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Exclusion Criteria

• Subjects for whom participation in the study may cause medical harm

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Telemedicine	Telemedicine follow-up visit	The patients selected to participate in the study are cervical dystonia (CD) patients who receive treatment at Vanderbilt University Medical Center, where the study takes place.

Primary Outcome Measures

Name	Time	Method
Patient Satisfaction with Telehealth	4 months	This questionnaire measures patient satisfaction with the telehealth visit scored 7 to 27

Trial Locations

Locations (1)

Vanderbilt University Medical Center; 🇺🇸 Nashville, Tennessee, United States