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NCT05617144 Clinical Trial

Aromatherapy Protocol for Pain Reduction in Hospice Patients

Pain Clinical Trial

Official title:
Aromatherapy Protocol for Pain Reduction in Hospice Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05617144
Other study ID # HSC-SN-21-1090
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 12, 2022
Est. completion date January 12, 2023

Study information
Verified date August 2023
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 6
Est. completion date January 12, 2023
Est. primary completion date January 8, 2023
Accepts healthy volunteers No
Gender All
Age group 50 Years to 99 Years
Eligibility Inclusion Criteria: - currently on hospice at Seasons Assisted Living Exclusion Criteria: - pain level not 3/10 or higher

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Aromatherapy treatment
60 minutes after pain medication administration primary investigator will turn on the diffuser (manufacture ScentSationals)and administer aromatherapy with a mixture of four drops of lavender and four drops of peppermint for 60 minutes.

Locations
Country Name City State
United States The University of Texas Health Science Center at Houston Houston Texas

Sponsors (1)
Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient satisfaction as assessed by the score on the Patient Satisfaction survey 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 end of study (7 days after baseline)
Secondary Change in pain as assessed by the score on the Wong Baker Face Scale (WBFPS) scale This is scored from 0(no hurt) to 10(hurts the worst) a higher number indicating more pain Baseline, 2 hours after every aromatherapy administration
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