Template:Further points for assessing the study: Difference between revisions
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==Sample== | ==Sample== | ||
{| class="wikitable" style="width: | {| class="wikitable" style="width:100%;" | ||
|- | |- | ||
! width= | ! width=70% style="text-align:left;" | Power analysis performed | ||
| style="text-align: | | style="text-align:left;" | [[power analysis performed::{{{power analysis performed|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Sample size corresponds to power analysis | ! style="text-align:left; text-indent:3em;" | - Sample size corresponds to power analysis | ||
| style="text-align: | | style="text-align:left;" | [[Sample size corresponds to power analysis::{{{Sample size corresponds to power analysis|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Reasons for insufficient sample size based on power analysis | ! style="text-align:left; text-indent:3em;" | - Reasons for insufficient sample size based on power analysis | ||
| style="text-align: | | style="text-align:left;" | [[Reasons given for samples being too small according to power analysis::{{{Reasons given for samples being too small according to power analysis|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | If no power analysis performed: at least moderate sample size (n >= 30 per arm) | ! style="text-align:left;" | If no power analysis performed: at least moderate sample size (n >= 30 per arm) | ||
| style="text-align: | | style="text-align:left;" | [[Samples sufficiently large::{{{Samples sufficiently large|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Ethnicity mentioned | ! style="text-align:left;" | Ethnicity mentioned | ||
| style="text-align: | | style="text-align:left;" | [[Ethnicity mentioned::{{{Ethnicity mentioned|}}}]] | ||
|} | |} | ||
==Alternative Explanation== | ==Alternative Explanation== | ||
{| class="wikitable" style="width: | {| class="wikitable" style="width:100%;" | ||
|- | |- | ||
! width= | ! width=30% style="text-align:left;" | Other explanations for an effect besides the investigated intervention | ||
| style="text-align: | | style="text-align:left;" | [[Other explanations for an effect besides the investigated intervention::{{{Other explanations for an effect besides the investigated intervention|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Possibility of attention effects | ! style="text-align:left; text-indent:3em;" | - Possibility of attention effects | ||
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|} | |} | ||
==Statistics== | ==Statistics== | ||
{| class="wikitable" style="width: | {| class="wikitable" style="width:100%;" | ||
|- | |- | ||
! width= | ! width=70% style="text-align:left;" | Correct use of parametric and non-parametric tests {{#info: Testing for normal distribution only necessary if parametric tests are used, NI: use of parametric tests without report of normal distribution testing| note}} | ||
| style="text-align: | | style="text-align:left;" | [[Correct use of parametric and non-parametric tests::{{{Correct use of parametric and non-parametric tests|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Correction for multiple testing | ! style="text-align:left;" | Correction for multiple testing | ||
| style="text-align: | | style="text-align:left;" | [[Correction for multiple testing::{{{Correction for multiple testing|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Measurement of compliance | ! style="text-align:left;" | Measurement of compliance | ||
| style="text-align: | | style="text-align:left;" | [[Measurement of compliance::{{{Measurement of compliance|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Consistent reporting in numbers (figures, flowchart, abstract, results) | ! style="text-align:left;" | Consistent reporting in numbers (figures, flowchart, abstract, results) | ||
| style="text-align: | | style="text-align:left;" | [[Consistent reporting in numbers::{{{Consistent reporting in numbers|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Comprehensive and coherent reporting | ! style="text-align:left;" | Comprehensive and coherent reporting | ||
| style="text-align: | | style="text-align:left;" | [[Comprehensive and coherent reporting::{{{Comprehensive and coherent reporting|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Cross-over | ! style="text-align:left;" | Cross-over | ||
| style="text-align: | | style="text-align:left;" | [[Cross-over::{{{Cross-over|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Sufficient washout period | ! style="text-align:left; text-indent:3em;" | - Sufficient washout period | ||
| style="text-align: | | style="text-align:left;" | [[sufficient washout period::{{{sufficient washout period|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Tested for carry-over effects | ! style="text-align:left; text-indent:3em;" | - Tested for carry-over effects | ||
| style="text-align: | | style="text-align:left;" | [[Tested for carry-over effects::{{{Tested for carry-over effects|}}}]] | ||
|- | |- | ||
! style="text-align:left; text-indent:3em;" | - Tested for sequence effects | ! style="text-align:left; text-indent:3em;" | - Tested for sequence effects | ||
| style="text-align: | | style="text-align:left;" | [[Were sequence effects tested::{{{Were sequence effects tested|}}}]] | ||
|} | |} | ||
==Interpretation of results== | ==Interpretation of results== | ||
{| class="wikitable" style="width: | {| class="wikitable" style="width:100%;" | ||
|- | |- | ||
! width= | ! width=70% style="text-align:left;" | Effect sizes reported (clinical vs. statistical significance) | ||
| style="text-align: | | style="text-align:left;" | [[Effect sizes reported::{{{Effect sizes reported|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Side effects systematically recorded | ! style="text-align:left;" | Side effects systematically recorded | ||
| style="text-align: | | style="text-align:left;" | [[Were side effects systematically recorded::{{{Were side effects systematically recorded|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Side effects considered in result interpretation | ! style="text-align:left;" | Side effects considered in result interpretation | ||
| style="text-align: | | style="text-align:left;" | [[Side effects taken into account in the interpretation of the results::{{{Side effects taken into account in the interpretation of the results|}}}]] | ||
|- | |- | ||
! style="text-align:left;" | Ethics votum | ! style="text-align:left;" | Ethics votum | ||
| style="text-align: | | style="text-align:left;" | [[Ethics / CoI / Funding::{{{Ethics / CoI / Funding|}}}]] | ||
|} | |} | ||
</includeonly> | </includeonly> | ||
Latest revision as of 12:09, 6 November 2024
This is the "Further points for assessing the study" template.
It should be called in the following format:
{{Further points for assessing the study
|Samples sufficiently large=
|power analysis performed=
|reasons given for samples=
|Ethnicity mentioned=
|Possibility of attention effects=
|Possibility of placebo effects=
|Other reasons=
|Testing for normal distribution=
|Correct application of statistical=
|Correction for multiple testing=
|Measurement of compliance=
|Blinding reliable=
|Check whether blinding was successful=
|Consistent reporting in numbers=
|Sufficient washout period=
|Tested for carry-over=
|Were sequence effects tested=
|Comprehensive and coherent reporting=
|Were side effects systematically recorded=
|Effect sizes reported=
|Side effects taken into account in the interpretation of the results=
|mono- or multicentric=
|Ethics / CoI / Funding=
}}
Edit the page to see the template text.