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Caregiver Experiences With Tracheostomy

Experiences of patıent's prımary Caregivers With Tracheostomy Suctioning Before Discharge

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05739578
Enrollment
11
Registered
2023-02-22
Start date
2021-12-01
Completion date
2022-02-20
Last updated
2023-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiver, Care Giving Burden, Tracheostomy

Keywords

Tracheostomy, Suctioning, Caregiver

Brief summary

This study aimed to determine the experiences of primary caregivers of patients with tracheostomies on tracheostomy suctioning procedure. This is a semi-structured qualitative study.

Detailed description

The study sample consisted of eleven (11) primary caregivers of patients with tracheostomies who were hospitalized in the otolaryngology clinic of a university hospital in a province located in the northwest of Turkey. This study was conducted using a semi-structured interview technique with the primary caregivers of the patients. Interviews were audio-recorded during the data collection procedure. The content of the audio recordings obtained during each interview was evaluated by the researchers using the content analysis method. The data were categorized, coded, and analyzed by creating themes and sub-themes. It was observed that the primary caregivers of the patients expressed fear, sadness, and anxiety during the suctioning procedure performed by healthcare professionals or themselves during their hospitalization. It was determined that caregivers need information on suctioning practice and insufficient knowledge on emergencies worries them as well.

Interventions

None listed

Sponsors

Uludag University
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Being a caregiver of patients with tracheostomy over the age of 18 * Volunteer. * Being the primary caregiver of the patient, * Ability to communicate verbally * Normal psychological state.

Exclusion criteria

* Being a caregiver of tracheostomy patients younger than 18 years of age * Rejecting the voluntary event, * Not being the primary caregiver of the patient, * Inability to communicate verbally * Having a psychological disorder

Design outcomes

Primary

MeasureTime frameDescription
Experiences of patient's primary caregivers with tracheostomy suctioning before dıschangeInterviews with each caregiver whose patient's discharge was planned lasted an average of 33 minutes. Interviews with a total of 11 caregivers were completed in 3 months.A data collection form included 12 questions related to the sociodemographic characteristics of patients and their primary caregivers. The semi-structured interview questions were as follows;1) How did you feel when the nurse/physician performed suctioning from the tube in your patient's throat for the first time? What did you think? 2) How did you feel when you heard that this process should be continued at home? What do you think? What was your reaction? 3)How did you feel when you performed tracheal suctioning for the first time? 4) What was your reaction when you first heard that suctioning will be your responsibility at home? 5)Are there any different topics/details you want to share related to tracheostomy suctioning before discharge?

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026