Clinical trial · Interventional
Does Acupressure Help Reduce Nausea and Vomiting in Palliative Care Patients? Formal Study
NCT00550251CI-TRIAL-00032773unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Nausea | — | UNRESOLVED | — |
| Vomiting | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Acupressure Wrist Bands (Sea-Bands) | Device | — | UNRESOLVED |
| Placebo wristbands | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Acupressure Bands
- description
- Elasticated wrist bands with active bead pressing on Pericardium 6 acupressure points bilaterally.
- interventionNames
- Device: Acupressure Wrist Bands (Sea-Bands)
- type
- PLACEBO_COMPARATOR
- label
- Placebo
- description
- Elasticated wrist bands without active bead.
- interventionNames
- Device: Placebo wristbands
Primary outcomes (1)
- measure
- Number of PRN Doses of anti-emetics needed
- timeFrame
- 3 days
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 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. 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 use of 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 taking part in the study. 6. Patients who are unable to read or comprehend the questionnaire or Visual Analogue Scale.
References
Publications (0)
Data not yet available
No reference posted for this study.