Table 4. Adverse events reported during the study.
FMI group | HMI group | Control group | P* | |
Any adverse event | 17 (33.3%) | 20 (39.2%) | 12 (24.0%) | 0.26 |
Upper respiratory infection | 6 (11.8%) | 4 (7.8%) | 5 (10.0%) | 0.80 |
Musculoskeletal pain | 3 (5.9%) | 5 (9.8%) | 2 (4.0%) | 0.49 |
Dizziness | 2 (3.9%) | 2 (3.9%) | 2 (4.0%) | 1.00 |
Contusion | 4 (7.8%) | 1 (2.0%) | 0 (0.0%) | 0.07 |
Dyspepsia | 2 (3.9%) | 2 (3.9%) | 1 (2.0%) | 0.82 |
Fracture | 1 (2.0%) | 1 (2.0%) | 2 (4.0%) | 0.76 |
Diarrhea | 2 (3.9%) | 2 (3.9%) | 0 (0.0%) | 0.37 |
Ligament injury | 2 (3.9%) | 1 (2.0%) | 1 (2.0%) | 0.78 |
Fall | 2 (3.9%) | 1 (2.0%) | 0 (0.0%) | 0.37 |
Values are shown as numbers (%). FMI, facility-based multidomain intervention; HMI, home-based multidomain intervention. *Chi-square test.