Is Acupuncture Able to Reduce Nausea and Vomiting in the Terminal Ill Patient
Primary Purpose
Terminal Illness
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Acupuncture
Sponsored by
About this trial
This is an interventional treatment trial for Terminal Illness focused on measuring Acupuncture, Nausea, Vomiting, Palliative care
Eligibility Criteria
Inclusion Criteria:
- Able to participate due to cognitive ability
- Nausea
- Admitted to in-bed hospice
Exclusion Criteria:
- Not able to participate due to cognitive impairment
- Lymphedema in the area of acupuncture site
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Acupuncture
Usual care
Arm Description
The intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Ying Tang were used.
Outcomes
Primary Outcome Measures
Change in nausea score
Using EORTC QLQ-c15-PAL, the nausea item. Values: not at all, a little, quite a bit, very much. Very much is the worse outcome
Change in vomiting
Unit of measure: Incidence of vomiting using the outcome measure question: Yes or No
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04378998
Brief Title
Is Acupuncture Able to Reduce Nausea and Vomiting in the Terminal Ill Patient
Official Title
Is Acupuncture Able to Reduce Nausea and Vomiting in the Terminal Ill Patient
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
January 25, 2015 (Actual)
Primary Completion Date
October 25, 2019 (Actual)
Study Completion Date
October 25, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A comparative effectiveness research design was used. The sample size was calculated to 136 patients, who were randomized to an intervention group and a control group respectively. The patients were terminal ill patients enrolled to three in-bed hospices in Denmark and nausea and vomiting were measured using EORTC QlQ-c15-PAL (European Organisation for Research and Treatment of Cancer, Quality of Life Questionaire, core 15, Palliation)
Detailed Description
The terminal ill patient is suffering from many different symptoms. In total 70% are suffering from nausea and vomiting due to the wide spread of cancer or due to side effects of treatment. Often the antiemetic's are not able to reduce symptoms to a level that enable the patient to experience quality in life in the last days of his life. The investigators had some experience with acupuncture as a complementary therapy but the investigators wanted more systematically to investigate if acupuncture is able to reduce the terminal ill patient´s nausea and vomiting. Literature show that acupuncture is able to reduce nausea and vomiting in patients receiving chemotherapy, but there is no literature that support the ability of acupuncture to reduce nausea and vomiting in the terminal ill patient.
The purpose of this study was to generate evidence based knowledge close to practice regarding the effect of acupuncture in reducing nausea and vomiting in the terminal ill patient.
Participants:
Terminal ill patients suffering from nausea and/or vomiting
Interventions:
The intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Yin Tang were used. The control group received usual care.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Terminal Illness
Keywords
Acupuncture, Nausea, Vomiting, Palliative care
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
136 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Acupuncture
Arm Type
Experimental
Arm Description
The intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Ying Tang were used.
Arm Title
Usual care
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Acupuncture
Intervention Description
The intervention group received usual care plus acupuncture for three days. The acupuncture spots: Pericardium-6, Stomach-36, Liver-3 and Yin Tang were used. The control group received usual care.
Primary Outcome Measure Information:
Title
Change in nausea score
Description
Using EORTC QLQ-c15-PAL, the nausea item. Values: not at all, a little, quite a bit, very much. Very much is the worse outcome
Time Frame
Change in nausea score from before intervention to three day after the intervention
Title
Change in vomiting
Description
Unit of measure: Incidence of vomiting using the outcome measure question: Yes or No
Time Frame
Change in vomiting from before intervention to four day after the intervention
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Able to participate due to cognitive ability
Nausea
Admitted to in-bed hospice
Exclusion Criteria:
Not able to participate due to cognitive impairment
Lymphedema in the area of acupuncture site
12. IPD Sharing Statement
Plan to Share IPD
No
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Is Acupuncture Able to Reduce Nausea and Vomiting in the Terminal Ill Patient
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