The Assessment of Movement Disorders Utilizing Live Two-Way Video

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Sandeep kapoor, North Shore Long Island Jewish Health System
ClinicalTrials.gov Identifier:
NCT01467089
First received: October 31, 2011
Last updated: September 21, 2015
Last verified: September 2015

October 31, 2011
September 21, 2015
November 2011
June 2016   (final data collection date for primary outcome measure)
  • Abnormal Involuntary Movement Scale (AIMS) when done in-person versus via two-way video [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  • Modified Simpson Angus Scale (mSAS) short version when done in-person versus via two-way video [ Time Frame: Baseline ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01467089 on ClinicalTrials.gov Archive Site
the correlation between the short version and full version of the Modified Simpson Angus Scale (mSAS) [ Time Frame: Baseline ] [ Designated as safety issue: No ]
total score of short version-Modified Simpson Angus Scale vs. total score of full version-Modified Simpson Angus Scale
Same as current
Not Provided
Not Provided
 
The Assessment of Movement Disorders Utilizing Live Two-Way Video
The Assessment of Movement Disorders Utilizing Live Two-Way Video
The purpose of this project is to determine the equivalency of extrapyramidal symptoms (EPS) and tardive dyskinesia (TD) examinations conducted via live two-way video versus live examinations completed in-person
Extrapyramidal symptoms (EPS) and tardive dyskinesia (TD) are one of the most frequent and troublesome adverse events when taking antipsychotic agents. The investigators aim in this study to determine if the investigators can conduct examinations for EPS and TD remotely using live two-way video. It is potentially beneficial for patients, especially those who are located far away from psychiatrists if they could be seen by trained clinicians and assessed for EPS and TD via two-way video in the future. Participants will be asked to have a medical assessment which consists of simple questions and some examination of their movements via two-way video and in person. The investigators will compare the results of video examinations with the results of live examinations.
Observational
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Not Provided
Not Provided
Non-Probability Sample
40 patients with schizophrenia will be recruited via in- and outpatient psychiatry service of The Zucker Hillside Hospital.
Tardive Dyskinesia
Other: Two way video assessment
Participants will be assessed extrapyramidal symptoms and tardive dyskinesia
schizophrenia

Inclusion Criteria: Inpatients and outpatients aged 18-75 years old who have been taking antipsychotics for longer than 6 months in their life time, and that have been compliant for the past week. Patients will be referred by their treating doctors if they have some evidence of movement disorder based on the physician's clinical judgment. We will also include 25% of the sample without any evidence of movement disorder.

Exclusion Criteria: Patients who have medical conditions which make it difficult to perform a physical examination. Patients who are clinically too ill to consent and/or unable to cooperate with the examination procedures.

Intervention: Other: Two way video assessment
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
40
June 2016
June 2016   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Inpatients and outpatients aged 18-75 years old who have been taking antipsychotics for longer than 6 months in their life time, and
  • That have been compliant for the past week.

Exclusion Criteria:

  • Patients who have medical conditions which make it difficult to perform a physical examination.
  • Patients who are clinically too ill to consent and/or unable to cooperate with the examination procedures.
Both
18 Years to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01467089
11-243B
No
Not Provided
Not Provided
Sandeep kapoor, North Shore Long Island Jewish Health System
Northwell Health
Not Provided
Principal Investigator: Sandeep Kapoor, MD Northwell Health
Northwell Health
September 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP