ISRCTN91640245
Completed
N/A
A randomised controlled trial to evaluate a novel CD-ROM learning package against the standard lecture - training system for research governance in the teaching of new researchers in an NHS Trust
Record Provided by the NHSTCT Register - 2007 Update - Department of Health0 sites30 target enrollmentSeptember 28, 2007
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Record Provided by the NHSTCT Register - 2007 Update - Department of Health
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Participants will be identified by obtaining lists of staff on Banding 6 \& 7 with research as part of their job description. These staff will then be approached by letter also enclosing a study information sheet. Participants will be recruited and consented on attendance at the lecture theatre for the teaching session.
- •Subject inclusion criteria:
- •1\. Age \> 18 years
- •2\. Able to give informed consent
- •3\. Research active
- •4\. Employee of the Cardiothoracic Centre \- Liverpool NHS Trust
- •The sample size has been calculated to detect a £2\.50 difference in cost using a 2 sample t test .at 90% power with a mean population wage of £ 20\.46 and a standard deviation of 1\.8\. This will be calculated by taking the direct costs of subject wages per hour spent learning and the unit cost of the teaching method. This provides a sample size of 24 (12 in each arm of the study). To allow for drop outs and to obtain 24 evaluable questionnaires a total of 30 subjects will be enrolled.
Exclusion Criteria
- •1\. Unable to take ½ day for teaching and follow\-up
- •2\. No access to computer
- •3\. Involved in another study within the last 30 days
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
N/A
An evaluation of a new resilience intervention for emergency workersISRCTN69644721niversity of Oxford255
Active, Not Recruiting
Phase 1
A randomised, controlled trial to investigate the effect of a four/six week intensified pharmacological treatment for schizophrenia, major depressive disorder and bipolar depression compared to treatment as usual in subjects who had a first-time treatment failure on their first-line treatment.Schizophrenia, schizoaffective disorder, schizophreniform disorder, major depressive disorder or bipolar disorder type I and II (currently in a depressive episode)MedDRA version: 20.0Level: HLTClassification code: 10039620Term: Schizoaffective and schizophreniform disorders Class: 10037175MedDRA version: 21.1Level: LLTClassification code: 10081270Term: Major depressive disorder Class: 10037175MedDRA version: 20.0Level: PTClassification code: 10039626Term: Schizophrenia Class: 100000004873MedDRA version: 21.1Level: LLTClassification code: 10004936Term: Bipolar depression Class: 10037175Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]CTIS2022-502185-24-00niversity Medical Center Utrecht1,254
Active, Not Recruiting
Phase 1
A randomised, controlled trial to investigate the effect of a six-week intensified pharmacological treatment for bipolar depression compared to treatment as usual in subjects who had a first-time treatment failure on their first-line treatment.Bipolar depressionMedDRA version: 21.1Level: LLTClassification code: 10004936Term: Bipolar depression Class: 10037175Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]CTIS2023-506605-19-00niversitair Medisch Centrum Utrecht423
Completed
Phase 4
A study to investigate the real-life use of the Vannair SMART regime in adult asthma (the SMART study).AsthmaRespiratory - AsthmaACTRN12610000515099Medical Research Institute of New Zealand300
Active, Not Recruiting
Phase 1
A randomised, controlled trial to investigate the effect of a six-week intensified pharmacological treatment for major depressive disorder compared to treatment as usual in subjects who had a first-time treatment failure on their first-line treatment.Major depressive disorderMedDRA version: 21.1Level: LLTClassification code: 10081270Term: Major depressive disorder Class: 10037175Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]CTIS2023-506617-21-00niversitair Medisch Centrum Utrecht418