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N/A Completed N=72 Randomized Supportive Care

Effect of Clear Masks on Patient Satisfaction With Communication

Communication · Patient Satisfaction
Source: ClinicalTrials.gov NCT05088603 ↗
Enrolled (actual)
72
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcomePrimary: Number of Participants With a Positive Response Score of 4 to Question 1 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire — 29; 29 Participants — p=0.106

Summary

The purpose of this research study is to evaluate participants' experience and satisfaction during the awake deep brain stimulation (DBS) procedure. Normally, the neurologist will ask the participant questions and also ask the participant to perform tasks during surgery. During this time, the neurologist will be talking to the participant and the participant will be responding by answering questions or participating with the tasks. For some study participants, there will be one small change made to the typical way the neurologist conducts this evaluation. The study staff will then ask the study participants about their experience with the neurologist's evaluation. The subject will not be told what part of the evaluation is changed for the study, until after they have responded to the questionnaire.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With a Positive Response Score of 4 to Question 1 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
29; 29 0.106
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 2 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
31; 33 0.99
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 3 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
28; 32 0.99
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 4 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
31; 34
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 5 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
31; 32 0.529
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 6 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
29; 32 0.99
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 7 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
29; 29 0.502
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 8 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
29; 30 0.431
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 9 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
27; 26 0.434
SECONDARY
Number of Participants With a Positive Response Score of 4 to Question 10 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
20; 17 0.159
SECONDARY
Number of Participants With a Positive Response to Question 11 on the Clinician & Group Survey-Consumer Assessment of Healthcare Providers and Systems (CG-CAHPS) Questionnaire
9; 2 0.051

Eligibility Criteria

Inclusion Criteria

  • Patients electing to undergo deep brain stimulator placement
  • Patient in whom general anesthesia is not planned for stimulator target localization

Exclusion Criteria

  • Patients who do not give consent
  • Patients who do not undergo DBS placement
  • Patients who are blind or have a severe visual impairment
  • Non-English speaking patients (i.e., patients for whom an interpreter would be needed to conduct the intra-operative assessment)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05088603). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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