Evaluation of Central Jugular Vein Catheter Lumen Holder Design and Ergonomic Use

NCT06375252 | Not Yet Recruiting

• 1 other identifier: sbughfyaseminozkan1985
• Study Type: interventional
• Target: 40
• Locations: 0 countries
• Sites: N/A

Brief Summary

The aim of this study was to evaluate the design and ergonomic use of central jugular vein catheter lumen holder.

Conditions

Central Venous Catheterization

Keywords

Design, Equipment; Nursing Research; Central Venous Catheterizations

Outcome Measures

Primary Outcomes (1)

• demographic information

  Contains participant identifying information

  10 minutes

Secondary Outcomes (1)

• comfort effect

  30 minutes

Study Arms (2)

intervention-control group

EXPERIMENTAL

Participants assigned to the intervention-control group of the study performed activities using the central jugular vein catheter lumen retainer apparatus.

Other: Central Jugular Vein Catheter Lumen Holder Apparatus

control-intervention group

NO INTERVENTION

Participants in the control-intervention group first performed the activities without the central jugular vein catheter lumen retainer apparatus, and then performed the activities with the apparatus.

Interventions

Central Jugular Vein Catheter Lumen Holder Apparatus OTHER

Participants will experience the central jugular vein catheter lumen holder apparatus, perform walking, sitting, supine, right and left side lying activities and fill out the evaluation forms prepared by the researcher. They will then experience the same activities without the apparatus.

intervention-control group

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Being a healthy individual over the age of 18
• Not having had a central jugular vein catheter inserted before for any reason (no experience)
• Being literate
• Voluntarily agreeing to participate in the research
• Being able to carry out daily life activities individually

You may not qualify if:

• Leaving work voluntarily
• Limitation in the head and neck area

Sponsors & Collaborators

• Saglik Bilimleri Universitesi: lead

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: HEALTH SERVICES RESEARCH
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: phd student

Study Record Dates

• First Submitted: April 16, 2024
• First Posted: April 19, 2024
• Study Start: April 19, 2024
• Primary Completion: May 16, 2024
• Study Completion: May 30, 2024
• Last Updated: April 19, 2024

Record last verified: 2024-04