Table A3.
Evidence Profile: SRV vs. Control on Functional Capacity: ADL | Evidence Profile: SRV vs. Control on Functional Mobility | ||||
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N° of studies: 8 (10 comparisons) Type of studies: RCT Intervention: Virtual Reality Systems on ADL Control: TPE, ADL, programs of health education or non-intervention N° of patients: 212 |
N° of studies: 22 (38 comparisons) Type of studies: RCT Intervention: Virtual Reality Systems Control: physical exercise, programs of health education or non-intervention N° of patients: 1097 |
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GRADE Factor | Importance | Explanations | GRADE Factor | Importance | Explanations |
Limitations in study design or execution (risk of bias) | Moderate ↓1 level |
Downgrading for risk of bias was not considered because most information is from studies at moderate risk of bias Moderate risk of bias Rate down one level |
Limitations in study design or execution (risk of bias) | Moderate ↓1 level |
Downgrading for risk of bias was not considered because most information is from studies at moderate risk of bias. Moderate risk of bias Rate down one level |
Inconsistency results | Serious ↓1 level |
Downgrading for inconsistency was considered because I2 = 79%. | Inconsistency results | No serious inconsistency | Downgrading for inconsistency was not considered because I2 = 58% |
Indirectness evidence | No serious indirectness | In none of the studies were there substantial differences between the population, intervention or outcomes measured in the studies and those established in the systematic review. | Indirectness evidence | No serious indirectness | In none of the studies were there substantial differences between the population, intervention or outcomes measured in the studies and those established in the systematic review. |
Imprecision | Moderated ↓1 level |
The OIS was calculated, the resulting OIS being 276 participants with MDS = 0.3. The number of patients included in the meta-analysis is 212, moderately lower to the OIS. Downgrading for imprecision was considered. |
Imprecision | No serious imprecision | The OIS was calculated, the resulting OIS being 276 participants with MDS = 0.3. The number of patients included in the meta-analysis is 1097, far superior to OIS. Downgrading for imprecision was not considered. |
Publication bias | Not serious | Downgrading for publication bias was not considered because the DOI plot shows no asymmetry with LFK = 0.36. |
Publication bias | Serious ↓1 level |
Downgrading for publication bias was considered because the DOI plot shows marked asymmetry with LFK = 3.3 (major asymmetry). |
Magnitude of effect | Moderated ↓1 level |
SMD = │0.31 │ Upgrading for large magnitude of effect was not considered. |
Magnitude of effect | Not serious | SMD =│0.58│ Upgrading for large magnitude of effect was not considered. |
Dose-response gradient | Not considered. | Dose–response gradient | Not considered. | ||
No plausible confounders | Not considered because studies in this meta-analysis are not observational. | No plausible confounders | Not considered because studies in this meta-analysis are not observational. | ||
Quality rating | Very low quality: we are moderately confident in the effect estimate; the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different (GRADE Working Group grades of evidence) | Quality rating | Moderate–low quality: we are moderately confident in the effect estimate; the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different (GRADE Working Group grades of evidence) |
Abbreviations: ADL: Activities of Daily Living; LFK: LFK Index; MCID: Minimum Clinically Important Difference; RCT: Randomized Controlled Trial; OIS: Optimal Information Size. VRS: Virtual Reality System.