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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
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Terminal Illness focused on measuring Acupuncture, Nausea, Vomiting, Palliative care

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    April 28, 2020
    Last Updated
    May 6, 2020
    Sponsor
    University of Aarhus
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    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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