Does Acupressure Help Reduce Nausea and Vomiting in Palliative Care Patients? Formal Study

Last updated: May 3, 2018
Sponsor: Sue Ryder Care
Overall Status: Active - Recruiting

Phase

N/A

Condition

Colic

Stomach Discomfort

Lactose Intolerance

Treatment

N/A

Clinical Study ID

NCT00550251
SRC2
  • Ages > 18
  • All Genders

Study Summary

Pilot study completed - power calculation performed. Now formal double blind randomized study comparing active with placebo wristbands for nausea in palliative care patients to be carried out.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Have a diagnosis of advanced cancer with an estimated prognosis of less than 1 yearbut more than 3 days.

  2. Describe their nausea as at least moderate on a Likert scale OR at have had at leastone vomit per day for the last three days.

  3. Have an underlying cause for their nausea which is thought to be irreversible OR thepatient has made an autonomous choice not to proceed with treatment for anypotentially reversible cause (for example surgery for obstruction or drainage ofascites).

  4. Can be male or female patients but must be over the age of 18.

  5. Have signed a consent form prior to entering the study.

  6. If patients are taking corticosteroids the dosage should be stable for 3 days beforeand during the trial.

  7. Be thought to be well enough to complete the 3 day trial.

Exclusion

Exclusion criteria:

  1. Arm lymphoedema.

  2. Weakness, fatigue or confusion sufficient that patient is unable to take part.

  3. Previous history of acupuncture/acupressure for nausea or vomiting, or history of useof acupressure by a close relative.

  4. History of Parkinsonism or Parkinsonism on examination.

  5. Patients will not be enrolled if they are sharing a room with another patient takingpart in the study.

  6. Patients who are unable to read or comprehend the questionnaire or Visual AnalogueScale.

Study Design

Total Participants: 58
Study Start date:
July 01, 2010
Estimated Completion Date:
July 31, 2018

Study Description

Terminally ill hospice in-patients suffering with nausea will be randomized to active or placebo acupressure bands. The study will last 3 days and they will be allowed to continue regular or have PRN anti-emetics during the study.

Assessors and patients will both be blinded to whether they patients are receiving active or placebo bands.

Connect with a study center

  • Sue Ryder Care Leckhampton Court Hospice

    Cheltenham, Gloucestershire GL53 0QJ
    United Kingdom

    Active - Recruiting

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