Can hypnosis decrease nausea and vomiting in a defined 3-day period in patients diagnosed with lymphoma or myeloma who are undergoing autologous bone marrow/stem cell transplantation?
| ISRCTN | ISRCTN84797116 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN84797116 |
| Protocol serial number | N0263120043 |
| Sponsor | Department of Health (UK) |
| Funder | University College London Hospitals NHS Trust (UK) |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 19/02/2014
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Mrs J Owens
Scientific
Scientific
UCH
Counselling & Complementary Team
Rosenheim Building
Grafton Way
London
WC1E 6AU
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Nausea and vomiting |
| Intervention | 1. Standard hypnotic technique 2. Self-hypnosis plus standard hypnotic technique |
| Intervention type | Other |
| Primary outcome measure(s) |
It is planned to use multiple t-tests to assess for significant differences in nausea and distress and vomiting levels between the hypnosis and relaxation groups. More power can be achieved by grouping all the data and it should be possible to look specifically for effects within each type of cancer group. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/06/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 60 |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 06/01/2003 |
| Date of final enrolment | 01/06/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
UCH
London
WC1E 6AU
United Kingdom
WC1E 6AU
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
