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. Author manuscript; available in PMC: 2011 Sep 15.
Published in final edited form as: Am J Drug Alcohol Abuse. 2011 Sep;37(5):426–433. doi: 10.3109/00952990.2011.596972

TABLE 5.

Retention analyses (n = 24).

Trial design characteristic (independent variable) Range Availability of the primary outcome measure(s)
Treatment exposure
Attendance at follow-up visits
Parameter estimate1 Test statistic (df) P-value Parameter estimate1 Test statistic (df) P-value Parameter estimate1 Test statistic (df) P-value
Type of intervention Medication −.161 F(2,21) = 3.36 .054 .023 F(2,21) = 1.63 .220 −.182 F(2,21) = 5.82 .010
Psychosocial .000 .000 .000
Combination .059 .132 −.037
Type of therapy Individual .000 F(2,21) = .05 .952 .000 F(2,21) = 8.78 .002 .000 F(2,21) = .14 .874
Group .005 −.247 .016
Combination −.021 .031 .029
Number of primary assessment sessions 1–12 −.010 t(22) = −.99 .331
Time of last primary assessment (days post-randomization) 11–365 −.0003 t(22) = −.84 .412
Number of treatment sessions 1–24 −.0001 t(22) = −.02 .987
Duration of treatment 1 day – 24 weeks2 .0000 t(22) = .01 .992
Number of CRF pages during treatment3 0–702 .0002 t(22) = 1.19 .248
Number of follow-up visits 1–8 −.005 t(22) = −.30 .766
Time of last follow-up visit (days post-randomization) 84–407 −.0003 t(22) = −1.16 .257
Number of CRF pages during follow-up visits3 10–203 .0003 t(22) = .65 .524

Notes:

1

Value of additional effect (for categorical variables in ANOVA) or of slope (for continuous variables in regression). For categorical variables (ANOVA), SAS sets the parameter value at 0 for the last category, after ordering the categories alphabetically.

2

In one trial, booster treatment sessions occurred up to 52 weeks post-randomization.

3

The amount of information collected on one case report form (CRF) page varies across instruments and trials.