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Table 1 Stakeholder ratings of interview derived outcomes

From: Methodology in core outcome set (COS) development: the impact of patient interviews and using a 5-point versus a 9-point Delphi rating scale on core outcome selection in a COS development study

  

Round 1

Round 2

Round 3

Survey

Survey

Survey

Outcome

Stakeholder Group

5 PT (%)a

9PT (%)a

5 PT (%)a

9PT (%)a

5 PT (%)a

9PT (%)a

Pain character/type

Clinician

77

67

81

83

82

72

 

Clinician/Researcher

61

40

68

43

42

29

 

Patient

90

73

86

83

70

63

 

Researcher

60

54

50

36

30

27

 

Service Provider/Policy Maker

100

67

100

80

67

80

Need for a Mobility Aid

Clinician

81

73

84

72

75

 

Clinician/Researcher

70

53

74

43

58

 

Patient

85

73

79

75

60

 

Researcher

80

46

60

64

20

 

Service Provider/Policy Maker

100

67

67

60

100

Perceived Body Imbalance

Clinician

47

56

26

34

 

Clinician/Researcher

48

33

26

29

 

Patient

70

68

57

58

 

Researcher

40

15

0

27

 

Service Provider/Policy Maker

100

17

33

40

Sexual Functioningb

Clinician

86

79

87

79

75

 

Clinician/Researcher

70

67

84

79

68

 

Patient

80

64

79

42

70

 

Researcher

80

69

70

73

70

 

Service Provider/Policy Maker

100

83

67

60

100

Family Life Impactb

Clinician

93

79

97

93

93

84

 

Clinician/Researcher

87

73

79

71

95

50

 

Patient

90

91

100

83

100

63

 

Researcher

90

85

100

73

100

64

 

Service Provider/Policy Maker

100

83

100

60

100

80

Social Life Impactb

Clinician

91

81

87

83

71

80

 

Clinician/Researcher

87

67

84

64

84

50

 

Patient

85

86

86

75

80

50

 

Researcher

80

85

90

82

90

55

 

Service Provider/Policy Maker

100

83

67

80

100

100

Emotional Symptomsb

Clinician

74

81

74

90

75

 

Clinician/Researcher

83

67

79

64

79

 

Patient

80

86

79

83

80

 

Researcher

90

77

70

55

70

 

Service Provider/Policy Maker

60

83

67

40

33

Frustration

Clinician

72

67

35

55

 

Clinician/Researcher

43

40

32

7

 

Patient

80

82

71

67

 

Researcher

40

23

40

27

 

Service Provider/Policy Maker

60

50

67

60

  1. a% of each stakeholder groups that rated the outcome as “important” on each scale (5 point and 9 point); (−) Indicates that the outcome did not go through to the corresponding Delphi survey round and subsequently was not rated by stakeholder groups; b Denotes outcomes that were included in the preliminary COS after round 3 of the Delphi