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Randomized Trial

maxytrejo1 Epid college Englisch 44 Karten

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  1. 1Randomized are imporant inevaluating for the prevention, dignosis, and treatment of disease
  2. 2RT can asnwer:more than one question at a time( factorial and other desighns)
  3. 3RT in some situations:can randomize entire groups ) communites, medical practices)
  4. 4In order to assess causal effects we shouldcontrast the outcome of people exposed to a risk factor with what would have happend in the absence of exposure
  5. 5The theoretically ideal way to assess what would have happened in the absence of exposure is termed the___counterfactual
  6. 6What is an imossible study desighnCompare the oucomses f a person exposed to a risk factor with the same person not exposed to the risk factor, at the same time and in the same place
  7. 7The closest we can come to such desighn isexperimental study
  8. 8What is the Evidence of Treatment Efficacy Hierarchy: (6)1.Anecdotal Case Reports 2.Case series w/o controls 3.Cross-sectional studies 4.Case-Control studies
    5.Longitudinal studies
    6.Randomized clinical trials
  9. 9An experimental study can determine: (2)If the factor prevents disease or if the therapeutic is an effect treatment
  10. 10What is the gold standardThe randomized trial is for assess the relationship between a therapeutic or clinical intervention and a disease outcome
  11. 11Another word for efficacy isinternal valididty
  12. 12One reason why we randomize:Self Selection to the treatment group is eliminated: studying the association between HTR and heart disease
  13. 13What is the second reason why we randomizePredictive factors (known and unknown) tend to be balances between intervention and comparison groups
  14. 14Predictive facotors:known factors have been assessed in the study, and unknown factors may affect the outcome. but have not been assess in the sudy
  15. 15THe observation studies of smoking cessation aids are fraught withselection biasis which typically deomstrates that the smoking cessation aids are ineffective( and selction bias)
  16. 16Explain the selection bias in smoking cessation studiesREaltionshps among use of cessation aids, nicotine dpendence and abistence are complicated: 3 self selcting groups
  17. 17In a RT the "current treatment can either__be given no treatment or the existing standard of care
  18. 18In RT the length of time between treatment and assessment will depend onwhat is being studied
  19. 19New treatment group=intervention group
  20. 20current treatment group=non intervention or control group
  21. 21In RT:There is defined population which will be randomized into a new treatment and current treatment and both into improved and not improved
  22. 22In an experiemtal study the advantage is that you canramdomize the intervention and no intervention group
  23. 23Rondomization is generally carried out usingcomupter generated random numbers
  24. 24For large studies, randomization should result in ____equal proportions of prognostic risk factor between the two groups, or also stratified randomization
  25. 25Validity of a randomized trial largely depends onsucess of the randomization process
  26. 26What is step one in stratifying randomizationStratify our study population by each variable that we consider important
  27. 27Step 2 in stratifying randomizationRandomize participants to treatment groups within each stratum
  28. 28In a double blinding Participants are__not aware of their intervention or treatment status
  29. 29In a double blinding Data collectors/analysts cannot___identify participants as being in the intervention or control groups
  30. 30In a DB: Study participantsdo not know which groups they are assighned to
  31. 31In a DB: Data collectors/ analystsdo not know which groups the patients have been assigned to when outcomes
  32. 32In a planed Cross over dseighn individualsswitch treatment and act as their own controls
  33. 33PCD is not possible iftherapy is surgical or cures the disease
  34. 34What are some precautions in a PCD:Carryover effects of one therapy into second therapy : may need a washout period
  35. 35a factorial randomized design is:A randomized trial design for evaluating 2 drugs or therapeutics "simultaneously" in the same study population
  36. 36a FRD can only be used ifthe anticipated outcomes of 2 drugs are "independent" and thier modes of action are "independent"
  37. 37Factorial Desighn example to assess preventive effects of1. Beta-Carotene on Cancer 2. Aspirin on myocardial infarction
  38. 38What is external valididtydetermined by how closely matched the study population is to the reference (or general) population
  39. 39Internal validity is determined byrandomization process, and is achieved when an observed difference (or lack of difference) in the treatment and control groups can be attributed to the treatment alone
  40. 40Externa validiy ( Generalizabilty) deals withRefernce population to the study population
  41. 41Internal validity deals withnew treatment and current treatment after they were randmized from te study population
  42. 42What are some units of group randomizationscommunities, small town, factories, schools, religious insitutions, chapters of social organizations, clinical practices
  43. 43Randomizing Groupsare less efficient statistically than randomization by individual
  44. 44In Randomized Groups the design and analysis must account forthe correlation of individuals within a group

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college Epid (Cross Sectional Study) Karteikarten am Randomized Trial, erstellt von maxytrejo1 am 22/05/2014.
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maxytrejo1
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