Table 1 –
Time 1 Assessment – Prior to Next Dose of Chemotherapy | |||||
---|---|---|---|---|---|
Model | LL | AIC | BIC | VLMR | Entropy |
2 Class | −13465.34 | 27032.68 | 27277.55 | 2375.10**** | .84 |
3 Classb | −13217.76 | 26589.51 | 26959.21 | 495.17**** | .83 |
4 Class | −13084.89 | 26375.78 | 26870.31 | 265.73ns | .80 |
Time 2 Assessment – Following the Next Dose of Chemotherapy | |||||
2 Class | −13286.83 | 26675.67 | 26920.53 | 2320.59**** | .83 |
3 Classb | −13021.47 | 26196.94 | 26566.64 | 530.73**** | .81 |
4 Class | −12892.35 | 25990.71 | 26485.24 | 258.23ns | .79 |
Not significant
p < .05
p < .01
p < .001
p < .0001
In order to have a sufficient number of patients with each symptom to perform the latent class analyses, the MSAS symptoms that occurred in at least 40% of the patients were identified. This criterion was selected to provide assurance that sufficient information was available to identify classes that were not sample-specific, due to infrequent reports of symptoms. A total of 25 out of 32 symptoms from the MSAS occurred in >40% of the patients.
The 3-class solution was selected because the VLMR was significant for the 3-class solution, indicating that three classes fit the data better than two classes, and the VLMR was not significant for the 4-class solution, indicating that too many classes had been extracted.
Note. LL = log-likelihood; AIC = Akaike Information Criterion, BIC = Bayesian Information Criterion; VLMR = Vuong-Lo-Mendell-Rubin likelihood ratio test for the K vs. K-1 model.