Health Literacy Clinical Trial
Official title:
Develop a Pictographic Educational Handouts and Validate Its Preliminary Efficacy on Tracheostomy Care
Verified date | December 2021 |
Source | Case Western Reserve University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of the study is to address the clinical problem of poor education outcome from the current practice of teaching tracheostomy care by providing them with a pictographic education handout to assist their learning. The study seeks to establish face validity and preliminary efficacy of a pictographic education handout with patients and identify factors associated with lower self-efficacy level on tracheostomy care.
Status | Completed |
Enrollment | 38 |
Est. completion date | May 30, 2021 |
Est. primary completion date | March 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years of age or older - Had a tracheostomy as part of head and neck cancer treatment, and who is not on mechanical ventilation - His or her date of the related tracheostomy surgery was within the past 6 months - Have received the discharge tracheostomy care education from the clinical nurse Exclusion Criteria: - Documented major physical or cognitive disabilities that would limit the ability to give informed consent or answer survey questions |
Country | Name | City | State |
---|---|---|---|
United States | Case Western Reserve University Frances Payne Bolton School of Nursing | Cleveland | Ohio |
Lead Sponsor | Collaborator |
---|---|
Case Western Reserve University | Sigma Theta Tau International Honor Society of Nursing, University Hospitals Seidman Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Author-developed self-efficacy on tracheostomy care scale | Participants' self-reported confidence on tracheostomy care from 0 to 10 (0="not confident", 10="very confident") | immediately after consenting and post intervention (up to 2 weeks) on study survey |
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