design choices for cluster randomised trials - alan girling

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Design Choices for Cluster-Randomised Trials Alan Girling University of Birmingham, UK [email protected] CLAHRC Scientific Advisory Group Birmingham, June 2015

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Page 1: Design choices for cluster randomised trials - Alan Girling

Design Choices for Cluster-Randomised Trials

Alan GirlingUniversity of Birmingham, UK

[email protected]

CLAHRC Scientific Advisory Group Birmingham, June 2015

Page 2: Design choices for cluster randomised trials - Alan Girling

… a Statistical viewpoint

• Ethical and Logistical concerns are suspended• RCTs and Parallel Cluster trials are well-

understood; ‘Stepped Designs’ less so.Two questions:1. How does the Stepped Wedge Design perform?…but The Genie is out of the bottle!2. What about alternative stepped designs?

Does it have to be a “Wedge”?

Page 3: Design choices for cluster randomised trials - Alan Girling

Some Alternative Designs:8 months 4 groups of Clusters (“Arms”)

Arms

1 1 1 1 1 1 1 1

1 1 1 1 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

Months

Arms

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

Months

Stepped-Wedge

Page 4: Design choices for cluster randomised trials - Alan Girling

Assumptions• Study of fixed duration (8 months)• Constant recruitment rate in each cluster• Continuous Outcome

– Additive treatment effect– Cross-sectional observations with constant ICC =

• Cross-over in one direction only (i.e. Treated to Control prohibited)• The analysis allows for a secular trend (“time effect”)

– This has been questioned; but if time effects are ignored, the ‘best’ statistical design involves simple before-and-after studies in each cluster (i.e. not good at all!)

Goal: To compare statistical performance of different designs under these assumptions, especially the Stepped-Wedge

Page 5: Design choices for cluster randomised trials - Alan Girling

1. ‘Precision Factor Plots’ for Comparing Designs

Page 6: Design choices for cluster randomised trials - Alan Girling

Clusters

1 1 1 1 1 1 1 1

1 1 1 1 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

Months

1. Simple Parallel Design

Two groups of clusters.Treatment implemented in one group only, in month 1.

Treatment Effect Estimate = (Mean difference between two groups over all months)

Two Simple Candidate Designs

Page 7: Design choices for cluster randomised trials - Alan Girling

Clusters

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

Months

1. Parallel Study with (multiple) baseline controls“Controlled Before-and-After Design”

Two groups of clusters.Treatment implemented in one group only, in month 5.

Treatment Effect Estimate = (Mean difference between two groups in months 5 – 8)

minusr x (Mean difference between two groups in months 1 – 4)

(r is a correlation coefficient “derived from the ICC”)

Page 8: Design choices for cluster randomised trials - Alan Girling

Performance measured by Precision of the effect estimate:Precision = 1/(Sampling Variance) = 1/(Standard Error)2

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

1 1 1 1 1 1 1 1

1 1 1 1 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

RN

4

1

2

1

14 2 RN

114 2

Precision =

Where R is the “Cluster-Mean Correlation”… and is the same for both designs

11

m

mR

(m = number of observations per cluster, = ICC)

CBA Parallel

Page 9: Design choices for cluster randomised trials - Alan Girling

Relative Efficiency of designs – by comparing straight lines on a Precision-Factor plot

CBA design is better (“more efficient”) if R > 2/3.Otherwise the Parallel design is better.

Parallel

CBA

Page 10: Design choices for cluster randomised trials - Alan Girling

2. The Cluster-Mean Correlation (CMC)

Page 11: Design choices for cluster randomised trials - Alan Girling

Cluster-Mean Correlation (CMC)

• Relative efficiency of different designs depends on cluster-size (m) and ICC (), but only through the CMC (R)

• The CMC (R) =proportion of the variance of the average observation

in a cluster that is attributable to differences between clusters

• (The ICC () = proportion of variance of a single observation

attributable to differences between clusters)• CMC can be large (close to 1) even if ICC is small

m

m

m

mR

111

Page 12: Design choices for cluster randomised trials - Alan Girling

Cluster-Mean Correlation: relation with cluster size

• CMC can be large (close to 1) even if ICC is small• So CBA can be more efficient than a parallel design for

reasonable values of the ICC, if the clusters are large enough

11

mR

R

Page 13: Design choices for cluster randomised trials - Alan Girling

3. Some other designs

Page 14: Design choices for cluster randomised trials - Alan Girling

1 1 1 1 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 0

0 0 0 0 0 0 0 0

Controlled Before & After Before & After + Parallel

R4

1

2

1 R

2

1

4

3

0 1 1 1 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

0 0 0 0 0 0 0 1

R32

9

16

9

0 1 1 1 1 1 1 1

0 0 0 1 1 1 1 1

0 0 0 0 0 1 1 1

0 0 0 0 0 0 0 1

R16

5

8

5

+ Baseline & Full Implementation Stepped Wedge

Precision Factors

Page 15: Design choices for cluster randomised trials - Alan Girling
Page 16: Design choices for cluster randomised trials - Alan Girling

• Stepped-Wedge is best when the CMC is close to 1• Parallel Design is best when the CMC is close to 0 – but risky if ICC

is uncertain• Before & After/Parallel mixture is a possible compromise

Parallel

Stepped-Wedge

B & A/Parallel

Page 17: Design choices for cluster randomised trials - Alan Girling

4. Is there a ‘Best’ Design?

Page 18: Design choices for cluster randomised trials - Alan Girling

• If Cross-over from Treatment to Control is permitted, the Bi-directional Cross-Over (BCO) design has Precision Factor = 1 at every R, better than any other design.

0 0 0 0 1 1 1 1

0 0 0 0 1 1 1 1

1 1 1 1 0 0 0 0

1 1 1 1 0 0 0 0R 01

Precision Factor =

• But this design is usually not feasible! • If ‘reverse cross-over’ is disallowed, the Precision Factor

cannot exceed2

3

11 RR

Page 19: Design choices for cluster randomised trials - Alan Girling

1 1 1 1 1 1 1 1

0 0 1 1 1 1 1 1

0 0 0 0 0 0 1 1

0 0 0 0 0 0 0 0

• Available design performance limited by choosing only 4 groups of clusters

Some (nearly) ‘Best’ designs with 4 groups of clusters

Stepped-Wedge

Parallel

RegionProhibited by Irreversibility of Intervention

Page 20: Design choices for cluster randomised trials - Alan Girling

1 1 1 1 1 1 1 11 1 1 1 1 1 1 10 1 1 1 1 1 1 10 0 0 1 1 1 1 10 0 0 0 0 1 1 10 0 0 0 0 0 0 10 0 0 0 0 0 0 00 0 0 0 0 0 0 0

Some (nearly) ‘Best’ designs with 8 groups of clusters

Stepped-Wedge

Parallel

Page 21: Design choices for cluster randomised trials - Alan Girling

‘Best’ Design for large studies: This is a mixture of Parallel and Stepped-Wedge clusters.

100R%Stepped-Wedge

Clusters

100(1 – R)%Parallel Clusters

• Includes Parallel and Stepped-Wedge designs as special cases• When R is close to 1 the Stepped-Wedge is the best possible

design

Page 22: Design choices for cluster randomised trials - Alan Girling

5. Conclusions

• Efficiency of different cluster designs depends on the ICC () and the Cluster-size (m) but only through the CMC (R).

• Precision Factor plots are useful for comparing designs– Comparisons are linear in R

• The Stepped-Wedge Design is most advantageous when R is close to 1.– In studies with large clusters this can arise even if the ICC is

relatively small.• The theoretically ‘best’ design choice is sensitive to R,

and combines Parallel with Stepped-Wedge clusters

Page 23: Design choices for cluster randomised trials - Alan Girling

Limitations

• Continuous data, simple mixed model– Natural starting point – exact results are possible– ?Applies to Binary observations through large-

sample approximations• Extension to cohort designs through nested

subject effects is straightforward and gives essentially the same answers