Recruitment to Trials. Background Recruitment of participants is a VERY important issue. The general consensus is that most trials under recuit.

Slides:



Advertisements
Similar presentations
Appraisal of an RCT using a critical appraisal checklist
Advertisements

How to write a study protocol Hanne-Merete Eriksen (based on Epiet 2004)
Recruitment to Clinical Trials: Adwoa Hughes-Morley What are the Strategies for Success?
Patient Preference and Comprehensive Cohort Designs.
Use of Placebos in Controlled Trials. Background The traditional ‘double-blind’ RCT uses a placebo to conceal allocation. There are a number of advantages.
Sample size issues & Trial Quality David Torgerson.
External Validity of Trials. Background External or ecological validity refers to whether the results of the trial can be generalised to the general clinical.
Robert Coe Neil Appleby Academic mentoring in schools: a small RCT to evaluate a large policy Randomised Controlled trials in the Social Sciences: Challenges.
Doug Altman Centre for Statistics in Medicine, Oxford, UK
‘Cohort multiple RCT’ design workshop Clare Relton & Jon Nicholl School of Health and Related Research (ScHARR) Faculty of Medicine University of Sheffield.
Health service utilization by patients with common mental disorder identified by the Self Reporting Questionnaire in a primary care setting in Zomba, Malawi.
Improving the Economic Efficiency of Clinical Trials.
Sources of Bias in Randomised Controlled Trials
What makes a good quality trial? Professor David Torgerson York Trials Unit.
Reading the Dental Literature
Journal Club Alcohol, Other Drugs, and Health: Current Evidence May–June 2013.
Subject Selection and Recruitment David Wendler Department of Clinical Bioethics NIH, USA.
Qualitative study on acceptability of screening Research team: Alison Heawood (PI, Bristol), Clare Emmett (Qualitative Researcher, Bristol), Niamh Redmond.
Doris Young, John Furler, Christine Walker, Margarite Vale, James Best, Leonie Segal, Trisha Dunning (NHMRC GP clinical research grant July ) PEACH:
Brandi Cooke Student Intern 3 rd National Summit on Preconception Health and Health Care June 12-14, 2011 Factors Affecting the Willingness of Counselors.
Cluster Randomised Trials. Background In most RCTs people are randomised as individuals to treatment. Whilst this method is appropriate for many interventions.
Cluster Randomised Trials. Background In most RCTs people are randomised as individuals to treatment. Whilst this method is appropriate for many interventions.
Clinical trials methodology group Simon Gates 9 February 2006.
How do nurses use new technologies to inform decision making?
Pragmatic Randomised Trials. Background Many clinical trials take place in artificial conditions that do not represent NORMAL clinical practice. Often.
Factorial Designs. Background Factorial designs are when different treatments are evaluated within the same randomised trial. A factorial design has a.
Pre-randomisation consent (Zelen’s method)
CKD Conservative care and preparation for dialysis UK Renal Registry 2013 Annual Audit Meeting Dr Anirudh Rao Registrar, UK Renal Registry.
Introduction to evidence based medicine
Achieving improved cancer outcomes- a pathway approach, engaging primary care and partners Kathy Elliott Programme Director – NHS Improving Quality (Delivery.
Critical Appraisal of Clinical Practice Guidelines
Are the results valid? Was the validity of the included studies appraised?
Implementation of local guideline by interactive workshop improves anticoagulation therapy and patient safety Puhakka J, Helsinki Health Centre, GP Suvanto.
18 th to 21 st June 2013 Primary Care Sciences Keele University RUNNING RANDOMISED CLINICAL TRIALS For further enquiries contact Debbie Cooke Tel: +44(0)1782.
Future research directions for patient safety in primary care Michel Wensing Wim Verstappen Sander Gaal.
Medical Audit.
Participants Adoption Study 109 (83%) of 133 WSU Cooperative Extension county chairs, faculty, and program staff responded to survey Dissemination & Implementation.
دکتر خلیلی 1. Lucid the way to “ Research” And Follow an “ Evidence Based Medicine”
Turning a clinical question into a testable hypothesis Lauren A. Trepanier, DVM, PhD Diplomate ACVIM, Diplomate ACVCP Department of Medical Sciences School.
Evidence Based Medicine Meta-analysis and systematic reviews Ross Lawrenson.
Repair of obstetric anal sphincter tears Journal Club 18 th February 2011 By Dr. Ian Haines GP-ST1 & Nevine te West.
Clinical equipoise & the RCT dilemma
POSTER TEMPLATES BY: Research Objective(s) Results Discussion References Introduction/Significance Study Procedures Specify.
EBC course 10 April 2003 Critical Appraisal of the Clinical Literature: The Big Picture Cynthia R. Long, PhD Associate Professor Palmer Center for Chiropractic.
Incidence of hospitalisations in both groups Incidence of documented infections Abstract Problem statement: Patients on cancer chemotherapy are at substantial.
Experimental studies Jean-François Boivin 25 October 2010.
FOLLOW-UP Simon Gates 13 April Contents Definition of follow-up Problems with follow-up Power Bias How much loss is acceptable? Prevention of losses.
Focusing the question Janet Harris Cochrane Qualitative Research Methods Group ESQUIRE Qualitative Systematic Review Workshop University of Sheffield 6.
SIPS in primary health care: extending the existing evidence base Professor Eileen Kaner.
How to read a paper D. Singh-Ranger. Academic viva 2 papers 1 hour to read both Viva on both papers Summary-what is the paper about.
A CONSENT DVD/ VIDEO DESIGNED TO IMPROVE CONSENT UPTAKE TO RANDOMISED CONTROLLED TRIALS IN NEONATOLOGY: A PILOT STUDY IN THE INIS NETWORK [VINIS] Priya.
How to Analyze Therapy in the Medical Literature (part 1) Akbar Soltani. MD.MSc Tehran University of Medical Sciences (TUMS) Shariati Hospital
Sifting through the evidence Sarah Fradsham. Types of Evidence Primary Literature Observational studies Case Report Case Series Case Control Study Cohort.
Randomised controlled trials in primary care: case study Doctor Sue Wilson University of Birmingham United Kingdom.
NIHR Themed Call Prevention and treatment of obesity Writing a good application and the role of the RDS 19 th January 2016.
How to Read a Journal Article. Basics Always question: – Does this apply to my clinical practice? – Will this change how I treat patients? – How could.
1 Lecture 10: Meta-analysis of intervention studies Introduction to meta-analysis Selection of studies Abstraction of information Quality scores Methods.
Arthritis Research UK Primary Care Centre Winner of the Queen’s Anniversary Prize For Higher and Further Education 2009 Recruiting patients and collecting.
1 6 th National Children & Young People Survivorship Workshop A GP perspective Una Macleod Professor of Primary Care Medicine Primary care cancer lead,
Developing a proposal Dónal O’Mathúna, PhD Senior Lecturer in Ethics, Decision-Making & Evidence
This study is funded by a contract from the National Cancer Institute, National Institutes of Health, U.S. Department of Health and Human Services. Cancer.
Title Investigators and sites. Clinical Trial Proposal Presentation Template for open forum at the 2017 ASM.
RUNNING RANDOMISED CLINICAL TRIALS
Design and Critique of Grants for Implementation Research
How to read a paper D. Singh-Ranger.
Randomized Trials: A Brief Overview
Lights! Camera! Graphs! Photos!
Pilot Studies: What we need to know
Survivorship Pathway Template
Study within a Trial (SWAT) to increase the evidence for trial recruitment and retention in decision making -Shaun Treweek From the UK Trial Managers.
Presentation transcript:

Recruitment to Trials

Background Recruitment of participants is a VERY important issue. The general consensus is that most trials under recuit.

Poor Recruitment Poor or slow recruitment to trials leads to the following problems: Increased risk of Type II error (concluding, erroneously there is no difference); Delay in implementing research findings; Research commissioners may seek other INFERIOR but quicker evaluative methods of research.

How common is the problem? There is little quantitative data to support the qualitative view that many trials under recruit. One study in USA noted that of 41 trials 34% failed to achieve sample size only another 34% got sample size on time.

Survey To ascertain whether poor trial recruitment was as poor as believed we undertook a survey of corresponding authors of a sample of trials published in 2000 and Puffer & Torgerson 2002;Unpublished

Method We identified all, individually, randomised trials published in the BMJ and Lancet years 2000 to Corresponding authors were ed a brief questionnaire asking about recruitment problems. One reminder was sent.

Results We ed 196 authors of individually randomised trials. 33 were bounced back from invalid addresses. We received 79 valid responses (48%).

Recruitment Problems

Recruitment Multicentred trials had significantly more problems than single centred studies (51% vs 23%; p = 0.02). Primary and Secondary trials had similar problems 43% and 39% primary vs secondary. No significant age difference 48 years vs 52 years for good recruiters vs poor recruiters.

Authors’ comments Facilitate Secondary care Use previously successful methods Few exclusion criteria large sampling frame Pilot study Hinder Competing with other trials. Ethics. Inaccurate incidence. Clinician resistance. Narrowly defined population.

Summary of Comments Recruitment is a problem in the MAJORITY of trials. Worse in multicentred trials. Need to use pilot studies. Need to use tried and tested strategies. Need to use large sampling frames.

Examples of poor recruitment York backpain trial needed 300 attained 180. MRC backpain needed 1300 (achieved target but needed extra funds and extended recruitment). Vein graft trial needed 1200 got 100 (trial collapsed). SAPPHIRE trial is under-recruiting.

DAMASK recruitment

Hip protector trial Aimed to recruit 4500 women at risk of hip fracture to wear hip protectors or act as controls. Used a combination of GP practices and publicity. Expected 10% pick up. Pilot showed 2.5%.

Other problems Hip protector trial was a multicentred study (orginally 5 centres). Two centres did not start on time, 1 was abandoned, the other started late and only got 50% of expected recruits.

What did we do? Increased eligibility criteria. Mailed out to more GPs Publicity Enrolled a 6 th Centre.

Hip Protector Trial

Calcium and D recruitment Again we recruited women with 1+ risk factors for hip fracture over 70 years. Again overestimated recruitment rates at 10%. Pilot showed a recruitment rate of 5%. We doubled the number of GPs to be included in study.

Other problems Calcium and D trial was a multicentred study. One centre was late in starting but eventually DID recruit its target.

Calcium and D trial

Recruiting Doctors Often recruting trial participants is only part of the problem need to recruit doctors as well. Primary care physicians, unlike secondary care doctors, do not have a career incentive to become involved in research.

GP recruitment Rate We paid both sets of GPs £50 to mail out prepaid envelopes. For calcium and D we also paid GPs £30 per patient randomised to active treatment. Required practice nurse to see patient for 20 minutes. Which trial recruited most GPs?

GP Recruitment

MRC RECORD Trial MRC RECORD trial recruited people from fracture clinics. Under recruited due to over optimistic recruitment predictions. BUT could not increase number of centres easily due to budget restraints.

What was done? Payment to trial centres was made conditional on recruitment rates. Initial contracts for 6 months of a research nurse. Poor performing centres were closed or finance was reduced. Trial extension sought and was given.

RECORD result RECORD trial will be late and not achieved initial sample size. Event rate was higher than expected so loss of power will not occur.

Evidence based recruitment? Not many RCTs of different methods of recruitment. Cooper et al, showed using a patient preference trial had not + or – effect on recruitment rates. RCT of nurses vs consultants for prostate cancer trial – no difference. RCT of trial co-ordinator visits to centres vs mailing recruitment packs in French cancer trial – no difference. Two open RCTs showed increase in recruitment. Education of GPs shows increase in recruitment Case control data of Zelen’s method does show increased recruitment rates.

Qualitative methods & recruitment Donovan and colleagues introduced a ‘rolling’ qualitative research process into patient recruitment for a trial on prostate cancer. Donovan et al. BMJ 2002;325:

Percent of eligible men recruited

Authors’ conclusions “Embedding the controversial ProtecT randomised trial within qualitative research allowed detailed investigation of the presentation of study information by recruiters and its interpretation by participants” “Changes to the content and delivery of study information increased recruitment rates from 40% to 70%”

Oh Dear As we ALL now know before and after studies CANNOT infer causality. Interesting data BUT we NEED an RCT to be sure that this intervention does improve recruitment rates. There is a natural tendency for recruitment rates to be poor at the start of a study anyway.

‘Natural’ changes in recruitment rates.

DAMASK monthly recruitment NB – no qualitative research intervention.

Recruitment Solutions? Assume from day 1 recruitment WILL be difficult and delayed. Find solutions from the beginning (e.g. extra ethics permission, loosening inclusion criteria). In multicentred trials tailor finance to each centre’s performance.

Summary Recruitment is an important issue. Most trials under-recruit. Careful attention needs to be paid to recruitment issues from the start.