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NCT02000245 Clinical Trial

Effects of Sympathy and Touch on Anxiety of Patients Undergoing Fiberoptic Bronchoscopy

Anxiety Clinical Trial

Official title:
Effects of Sympathy and Touch on Anxiety of Patients Undergoing Fiberoptic Bronchoscopy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02000245
Other study ID # STAF
Secondary ID 1307-042-504
Status Completed
Phase N/A
First received November 20, 2013
Last updated April 18, 2016
Start date October 2013
Est. completion date December 2014

Study information
Verified date April 2016
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of verbal expression of sympathy and touch on anxiety of patients undergoing fiberoptic bronchoscopy

Recruitment information / eligibility
Status Completed
Enrollment 267
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

- adult patients undergoing diagnostic fiberoptic bronchoscopy

- hospitalized patients

Exclusion Criteria:

- patients who have undergone fiberoptic bronchoscopy

- not hospitalized patients

- cognitive impairment

- refusal to enroll

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Intervention

Behavioral:
• verbal expression for compassion
The doctor going to perform bronchoscopy tells a short sentence to a patient. (Hello, I'm Dr.OO. During this test, I will keep an eye on you. Don't worry)
• touch
The doctor going to perform bronchoscopy puts a hand on the patient's shoulder

Locations
Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary change of visual analogue scale (VAS) for anxiety baseline (arrival at the test room), and follow-up (at least 10 min after baseline, right before undergoing bronchoscopy No
Secondary Satisfaction of patients after fiberoptic bronchoscopy within 6 hours after bronchoscopy No
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