Clinical Trials Directory

Trials / Completed

CompletedNCT05696899

Determining the Efficacy of Essential Oil Aromatherapy in Children Undergoing Port Access

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
4 Years – 18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if the use of aromatherapy impacts patient anxiety and pain scores surrounding port access in pediatric oncology patients between the ages of 4 years and 18 years.

Detailed description

Specific aims include the following: Aim 1: To compare pre and post port access anxiety scores for both control and intervention groups. Aim 2: To assess pre and post port pain scores surrounding port access for both control and intervention groups. Aim 3: To compare pain and anxiety scores between age groups. The overall goal of this pilot study is to identify if aromatherapy, using non-topical, STILL QuickTAB Medipack blended scent aromatherapy, manufactured by Soothing Scents, is effective as a valid non-pharmacologic supplementation in reducing anxiety and pain scores during port access in pediatric oncology patients.

Conditions

Interventions

TypeNameDescription
OTHERSTILL QuickTAB Medipack blended scent aromatherapy, manufactured by Soothing ScentsA resealable quick-tab dispenser with the 'therapeutic inhaled essential oils' lavender, bergamot, sweet orange, and ylang ylang.

Timeline

Start date
2023-12-05
Primary completion
2024-05-30
Completion
2024-05-30
First posted
2023-01-25
Last updated
2024-12-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05696899. Inclusion in this directory is not an endorsement.