Trial Information

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

Pilot The study will be piloted with 10 patients to ensure that the protocol is acceptable
to patients and to inform a formal power calculation for a larger study. Patients will be
randomized to each arm according to a randomization programme at www.randomization.com.

Arm 1 Instruction and placement of acupressure bands at the P6 acupuncture point
bilaterally. This point is located 2 cun (a Chinese measurement equal to approximately 3cm)
proximal to the midpoint of the transverse crease of the wrist between the tendons of
palmaris longus and flexor carpi radialis.

Arm 2 Instruction and placement of sham acupressure bands P6 acupuncture point bilaterally.
Sham acupressure bands have no stud to stimulate P6.

Patients may choose to have regular anti-emetics or a subcutaneous syringe driver after 24
hours if they are not happy with their level of nausea and vomiting.

4. STUDY POPULATION

4.1 Source and Number of Patients: Hospice in-patients. 10 patients for pilot.

4.2 Inclusion Criteria

Patients must meet the following criteria to be eligible to participate in the study:

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

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

3. Have an underlying cause for their nausea which is thought to be irreversible OR the
patient has made an autonomous choice not to proceed with treatment for any potentially
reversible cause (for example surgery for obstruction or drainage of ascites).

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 before
and during the trial.

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

4.3 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.

4. History of Parkinsonism or Parkinsonism on examination.

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

5. OUTCOME MEASURES

1. Visual Analogue Scale of nausea measured every 6 hours. If patients are asleep they
will not be waken for assessments overnight.

2. Duration of perceived nausea over preceding time period.

3. Number of vomits per 24 hours.

4. Volume of vomit per 24 hours.

5. Adverse effects of acupressure.

6. Number of doses of PRN anti-emetics.

7. Measure of whether the patient felt the intervention helped at the end of the trial.

6. QUANTITATIVE ANALYSIS

This pilot will allow a formal power calculation to be performed to elucidate how many
patients need to be randomized to the full study.

Statistical analysis will be performed by Sarah Vowler at the Centre for Applied Medical
Statistics.