Implementation of an evidence based smoking cessation strategy (SMOCC) for patients with COPD in primary care
| ISRCTN | ISRCTN52757029 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN52757029 |
| ClinicalTrials.gov (NCT) | NCT00294905 |
| Protocol serial number | N/A |
| Sponsor | University Medical Center St. Radboud, Centre for Quality of Care Research (WOK) (The Netherlands) |
| Funder | Netherlands Organisation for Health Research and Development (ZonMw) |
- Submission date
- 14/02/2006
- Registration date
- 14/02/2006
- Last edited
- 25/10/2022
- Recruitment status
- No longer recruiting
- Overall study status
- Stopped
- Condition category
- Respiratory
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 J.E. Jacobs
Scientific
Scientific
University Medical Centre St. Radboud
Kwaliteit van Zorg
P.O. Box 9101
Nijmegen
6500 HB
Netherlands
| Phone | +31 (0)24 3615310 |
|---|---|
| j.jacobs@kwazo.umcn.nl |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | - |
| Study objectives | The large implementation of SMOCC will be more (cost-)effective than the usually applied basic dissemination strategies for guidelines. |
| Ethics approval(s) | Ethics approval received from the local medical ethics committee |
| Health condition(s) or problem(s) studied | Chronic Obstructive Pulmonary Disease (COPD), smoking. |
| Intervention | Large scale implementation of a combined strategy, aimed at the complete GP practice team (education by consultant at the practice, help with detecting smoking COPD patients, supplying materials for patient education, helpdesk/website, reminders by e-mail and phone) versus usual care. |
| Intervention type | Other |
| Primary outcome measure(s) |
Primary outcome measures will be biochemically validated smoking abstinence at 12 and 18 months. |
| Key secondary outcome measure(s) |
Secondary outcome measures will be counseling contacts and counseling behaviour of professionals and cessation attempts of patients. |
| Completion date | 01/11/2008 |
| Reason abandoned (if study stopped) | Participant recruitment issue |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 2700 |
| Key inclusion criteria | 1. COPD 2. Smoking 3. Age 40 or more |
| Key exclusion criteria | 1. Under control of lung specialist 2. Not Dutch-speaking 3. Serious physical or psychiatric comorbidity 4. Age under 40 |
| Date of first enrolment | 01/01/2006 |
| Date of final enrolment | 01/11/2008 |
Locations
Countries of recruitment
- Netherlands
Study participating centre
University Medical Centre St. Radboud
Nijmegen
6500 HB
Netherlands
6500 HB
Netherlands
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan | Not provided at time of registration |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | 01/11/2005 | Yes | No |
Editorial Notes
25/10/2022: Internal review.
14/02/2019: Publication reference added.
23/09/2010: Clinicaltrials.gov stated that this trial was terminated by September 2010 due to insufficient recruitment.
