- Pre-registration of Studies: Registering study protocols in advance can prevent selective reporting. Platforms like ClinicalTrials.gov are useful for this purpose. - Blinding: Blinding participants, data collectors, and analysts can reduce observer and social desirability biases. - Standardized Reporting Guidelines: Adhering to guidelines such as CONSORT for clinical trials or STROBE for observational studies ensures comprehensive reporting. - Open Access to Data: Encouraging data sharing and transparency can help verify results and reduce selective reporting.
