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Improving Surgical Patient Knowledge and Safe Use of Opioids

University Health Network, Toronto logo

University Health Network, Toronto

Status

Completed

Conditions

Opioid Use

Treatments

Other: Educational pamphlet arm

Study type

Interventional

Funder types

Other

Identifiers

NCT03629314
18-5723

Details and patient eligibility

About

Opioids are commonly prescribed for surgical patients to treat moderate to severe pain after surgery. However, opioids can be associated with serious complications such as respiratory depression and death. Currently, it is not routine practice to educate surgical patients about the risks of opioids and how to safely use opioids after surgery. The investigators have developed an educational pamphlet specifically for surgical patients to educate them about the safe use of opioids. The objective of this pilot study is to determine the usability and readability of an educational pamphlet about the safe use, proper storage and disposal of opioids. The educational pamphlet will be modified based on the feedback from the pilot study and subsequently used for a randomized controlled trial.

Full description

Twenty participants presenting to the preoperative clinic will be recruited for the pilot study. After informed consent is obtained, patients will be given an opioid knowledge questionnaire to complete before the education. They will then be given an educational pamphlet to review. After they have reviewed the educational pamphlet, they will complete the same opioid knowledge questionnaire. They will also complete a questionnaire evaluating the patient educational pamphlet. The pamphlet will be modified based on the feedback from the patients in the pilot study.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ≥18 years adults
  2. Proficient in English
  3. scheduled for elective surgery

Exclusion criteria

  1. Patients who are on opioids for chronic pain
  2. Patients have taken opioids in the past 30 days
  3. Patients who are unable to read and understand English -

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Educational Pamphlet arm
Experimental group
Description:
Educational Pamphlet will be provided to all participants to review, questionnaire will be provided to complete before and after review of the pamphlets
Treatment:
Other: Educational pamphlet arm

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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