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The effect of nursing consultation on anxiety, tolerance and satisfaction in patients undergoing colonoscopy

Not Applicable
Conditions
Anxiety.
Generalized anxiety disorder
Registration Number
IRCT2013022011936N2
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
74
Inclusion Criteria

age between 18 -75 years old; the ability to understand the Persian language; lacking a history previous colonoscopy; lack known history of psychological problems or anxiety disorders (According to the survey patient records ); lack of use sleep medications and sedatives on the day before colonoscopy; lack of severe pain due to the nature of the disease (for example cancer); lack of narcotic addiction or strong analgesics and absence of disease or a history of hypertension and antihypertensive drugs.
Exclusion criteria: canceled on the day of colonoscopy to determine the cause of non-anxious patients and patient withdrew from participating the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anxiety. Timepoint: Before intervention - a day after the intervention (before the procedure). Method of measurement: Spielberger standard questionnaire.
Secondary Outcome Measures
NameTimeMethod
Tolerance. Timepoint: After Colonoscopy. Method of measurement: The Likert scale measure.;Satisfaction. Timepoint: After Colonoscopy. Method of measurement: Numerical scale (1 least satisfied - 10 most satisfied).;Comfort. Timepoint: After Colonoscopy. Method of measurement: Comfort numerical scale (1 lowest Comfort, 10 maximum comfort level).;Cooperation rates during colonoscopy. Timepoint: After Colonoscopy. Method of measurement: Numerical scale contribution (1 co lowest, 10 the highest level of cooperation).;Pain. Timepoint: After Colonoscopy. Method of measurement: numeric pain scale (1 least amount of pain, 10 maximum pain).
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