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NCT05696899 · ClinicalTrials.gov registry record · NA
Determining the Efficacy of Essential Oil Aromatherapy in Children Undergoing Port Access
A NA study, sponsored by Stanford University.
- Completed
- Registry status
- NA
- Development phase
- 23
- Enrollment target
NCT05696899: Completed NA study, sponsored by Stanford University.
NCT05696899 is a NA study that has completed, run by Stanford University. The registered enrollment target is 23 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05696899, a NA study, has completed, sponsored by Stanford University.
- COMPLETED
- Registry status
- NA
- Development phase
- 23 participants
- Enrollment target
Study 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.
Primary Outcome
Comparison of pre and post patient anxiety scores for both control and intervention groups using the Visual Facial Anxiety Scale with corresponding values ranging from 0-10. 0 indicates no anxiety and 10 indicates the highest level of anxiety. Anxiety score will be measured by using the Visual Facial Anxiety Scale (VFAS)
Interventions
- OTHER STILL QuickTAB Medipack blended scent aromatherapy, manufactured by Soothing Scents
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2023-12-05 |
| Est. Completion | 2024-05-30 |
| Phase | NA |
What the finished NCT05696899 record still lists
NCT05696899 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 1 intervention - of which STILL QuickTAB Medipack blended scent aromatherapy, manufactured by Soothing Scents is the first listed.
NCT05696899 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05696899 about?
NCT05696899 is a clinical study titled "Determining the Efficacy of Essential Oil Aromatherapy in Children Undergoing Port Access". 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.
What is the current status of trial NCT05696899?
This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2023-12-05. Estimated completion is 2024-05-30.
What interventions are being tested in trial NCT05696899?
The interventions under investigation include: STILL QuickTAB Medipack blended scent aromatherapy, manufactured by Soothing Scents (OTHER).
Who is sponsoring clinical trial NCT05696899?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05696899's enrollment target sits among peer trials
23 1755th of 2000 higher than 245 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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