Hypnosis and self-hypnosis, administered and taught by nurses, for the reduction of chronic pain: a controlled clinical trial
| ISRCTN | ISRCTN32129167 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN32129167 |
| Protocol serial number | N/A |
| Sponsor | Hospital of Morges (Switzerland) |
| Funder | Swiss National Science Foundation (Switzerland) (SNF 4034-35883) |
- Submission date
- 06/09/2005
- Registration date
- 04/10/2005
- Last edited
- 10/09/2009
- 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
Dr Bernard Burnand
Scientific
Scientific
IUMSP
Bugnon 17
Lausanne
CH-1010
Switzerland
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Hypnosis and auto-hypnosis do not reduce pain in patients with chronic pain |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Various conditions engendering chronic pain |
| Intervention | Hypnosis and auto-hypnosis administered and taught by trained nurses |
| Intervention type | Other |
| Primary outcome measure(s) |
Level of pain (VAS) |
| Key secondary outcome measure(s) |
1. Physical activity (tridimensional accelerometer) |
| Completion date | 31/12/1994 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Sex | All |
| Target sample size at registration | 130 |
| Key inclusion criteria | 1. To be referred (including occasional self-referral) for the management of chronic pain 2. To live within manageable distances from the hospital 3. To be aged 18 or above 4. To understand and speak French adequately 5. To be able to see, hear and communicate (i.e. no alteration of consciousness) 6. To have no diagnosis of mental illness (e.g. psychosis) 7. To give informed consent |
| Key exclusion criteria | Patients were excluded from the study whenever they wished and/or when no conventional treatment could be proposed. |
| Date of first enrolment | 01/05/1993 |
| Date of final enrolment | 31/12/1994 |
Locations
Countries of recruitment
- Switzerland
Study participating centre
IUMSP
Lausanne
CH-1010
Switzerland
CH-1010
Switzerland
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Protocol article | protocol | 01/08/1994 | Yes | No |