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Aromatherapy Protocol for Pain Reduction in Hospice Patients

Not Applicable
Completed
Conditions
Pain
Interventions
Other: Aromatherapy treatment
Registration Number
NCT05617144
Lead Sponsor
The University of Texas Health Science Center, Houston
Brief Summary

The purpose of this study is to introduce aromatherapy with current pain medication protocols to see if it improves patient satisfaction and reduces pain in hospice care patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6
Inclusion Criteria
  • currently on hospice at Seasons Assisted Living
Exclusion Criteria
  • pain level not 3/10 or higher

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
TreatmentAromatherapy treatment-
Primary Outcome Measures
NameTimeMethod
Patient satisfaction as assessed by the score on the Patient Satisfaction surveyend of study (7 days after baseline)

This survey has 4 questions and each is scored from 1(strongly disagree) to 5(strongly agree) for a maximum score of 20, a higher score indicating more satisfaction

Secondary Outcome Measures
NameTimeMethod
Change in pain as assessed by the score on the Wong Baker Face Scale (WBFPS) scaleBaseline, 2 hours after every aromatherapy administration

This is scored from 0(no hurt) to 10(hurts the worst) a higher number indicating more pain

Trial Locations

Locations (1)

The University of Texas Health Science Center at Houston

🇺🇸

Houston, Texas, United States

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