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Clinical Trials/NCT03807960
NCT03807960CompletedNot Applicable

The Effect of Visual and Written Information Tools on Patient Controlled Analgesia Device Usage

Tuğba Karaman2 sites in 1 country96 target enrollmentStarted: February 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
96
Locations
2
Primary Endpoint
Pain Score

Study Overview

Brief Summary

This study is aimed to show the effect of information method on properly usage of the patient controlled analgesia(PCA) device

Detailed Description

Postoperative pain is still a challenge for anesthesiologist. Patient controlled analgesia is an effective method for postoperative pain management. However, most of the patient can not use the device properly. The important cause of inabilities about device usage is insufficient information.In the patient information, visual, oral or written communication methods can be chosen. However, which method is suitable for our patient group is not clear.This study is aimed to show the effect of information method on properly usage of the patient controlled analgesia(PCA) device

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • informed consent
  • Elective hysterectomy

Exclusion Criteria

  • Opioid abuse or Chronic opioid usage
  • opioid allergy
  • obesity(BMI>30)
  • psychiatric disease
  • more than American Anesthesiologist Score 2

Arms & Interventions

control

Other

The anesthesiologist will describe the PCA usage as in the routine care to the control group patients.

Intervention: routine care (Other)

visual

Experimental

The video about patient controlled analgesia device (PCA) usage will shown to the patients via notebook.

Intervention: video (Other)

written

Experimental

The written form which include the same knowledge will give to the patient for reading.

Intervention: written form (Other)

Outcomes

Primary Outcomes

Pain Score

Time Frame: At postoperative 24th hours.

Numeric rating scale (0 to 10) will be used for postoperative pain score

Secondary Outcomes

  • Postoperative analgesic consumption(Up to the postoperative 24th hours.)
  • PCA device demand dose duration(During postoperative 24hours)
  • PCA device usage(During postoperative 24 hours)
  • Patient's satisfaction(At the postoperative 24th hours)
  • The change of the postoperative pain score(Up to the postoperative 24th hours.)

Investigators

Sponsor
Tuğba Karaman
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Tuğba Karaman

Associate Professor,MD

Tokat Gaziosmanpasa University

Study Sites (2)

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