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  1. Submit a detailed research proposal to an Institutional Ethics Committee (IEC) of KAHER for review and approval. Contact your Guide/Supervisor to help you with it. It takes time to receive approvals, and there are chances that you need to amend to receive an approval, so plan well in advance to ensuRead more

    Submit a detailed research proposal to an Institutional Ethics Committee (IEC) of KAHER for review and approval. Contact your Guide/Supervisor to help you with it. It takes time to receive approvals, and there are chances that you need to amend to receive an approval, so plan well in advance to ensure you do not get late in your research start-up.

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  2. Consult your Guide/Supervisor. You can also seek assistance from the R & D Cell. Please select journals with higher impact factor, that you are referring or will refer/ referred in your research. Plan it well in advance. Once your journal is selected, follow journal guidelines, including structuRead more

    Consult your Guide/Supervisor. You can also seek assistance from the R & D Cell. Please select journals with higher impact factor, that you are referring or will refer/ referred in your research. Plan it well in advance. Once your journal is selected, follow journal guidelines, including structured sections like introduction, methods, results, discussion, and conclusion.

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  3. It is best to consult with your Guide/Supervisor. You can also seek assistance from the R & D Cell. Please select journals with higher impact factor, that you had referred in your research. Plan it well in advance. Choose appropriate peer-reviewed journals relevant to your field, considering impRead more

    It is best to consult with your Guide/Supervisor. You can also seek assistance from the R & D Cell. Please select journals with higher impact factor, that you had referred in your research. Plan it well in advance. Choose appropriate peer-reviewed journals relevant to your field, considering impact factor and readership.

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  4. Ethical and regulatory approvals, patient recruitment, clinical trial liability insurance, compliance, potential side effects, need for clinical expertise.

    Ethical and regulatory approvals, patient recruitment, clinical trial liability insurance, compliance, potential side effects, need for clinical expertise.

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  5. Engage patients in the research process, consider their perspectives, and prioritize their needs.

    Engage patients in the research process, consider their perspectives, and prioritize their needs.

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  6. : Descriptive statistics (mean, median, mode, standard deviation), hypothesis testing, p-values, confidence intervals, correlation analysis, regression analysis, survival analysis, and appropriate statistical tests based on study design (t-test, ANOVA, chi-square test). 

    : Descriptive statistics (mean, median, mode, standard deviation), hypothesis testing, p-values, confidence intervals, correlation analysis, regression analysis, survival analysis, and appropriate statistical tests based on study design (t-test, ANOVA, chi-square test). 

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  7. Consider the type of data (numerical, categorical), study design (experimental, observational), research question, and the number of variables involved. Consult a statistician at KAHER, if needed. Please discuss with your Guide/Supervisor. You may also contact R & D Cell to help you facilitate tRead more

    Consider the type of data (numerical, categorical), study design (experimental, observational), research question, and the number of variables involved. Consult a statistician at KAHER, if needed. Please discuss with your Guide/Supervisor. You may also contact R & D Cell to help you facilitate this. 

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  8. This answer was edited.

    Clear study protocol, well-defined inclusion/exclusion criteria, appropriate sample size calculation, accurate data collection methods, and data quality checks. We suggest you develop ‘Data Collection Forms (DCF)’, and get this reviewed by your Guide/Supervisor, so that your collection of data is plRead more

    Clear study protocol, well-defined inclusion/exclusion criteria, appropriate sample size calculation, accurate data collection methods, and data quality checks. We suggest you develop ‘Data Collection Forms (DCF)’, and get this reviewed by your Guide/Supervisor, so that your collection of data is planned and managed properly. Remember that ‘no data leads to no research’, and all data must be ALCOA-C compliant.

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  9. A p-value indicates the probability of observing a result at least as extreme as the one observed, assuming the null hypothesis is true. A confidence interval provides a range of values within which the true population parameter is likely to fall with a certain level of confidence.  

    A p-value indicates the probability of observing a result at least as extreme as the one observed, assuming the null hypothesis is true. A confidence interval provides a range of values within which the true population parameter is likely to fall with a certain level of confidence.  

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  10. A p-value indicates the probability of observing a result at least as extreme as the one observed, assuming the null hypothesis is true. A confidence interval provides a range of values within which the true population parameter is likely to fall with a certain level of confidence.  

    A p-value indicates the probability of observing a result at least as extreme as the one observed, assuming the null hypothesis is true. A confidence interval provides a range of values within which the true population parameter is likely to fall with a certain level of confidence.  

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