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Table 2 Reasons not to participate in the consecutive recruitment phases

From: Randomized double-blind placebo-controlled trial of sublingual immunotherapy in children with house dust mite allergy in primary care: study design and recruitment

Letter returned (n = 1483)

  

Reasons not to participate

Total

(n)

Percentage

Few or no complaints

710

48.4%

Other allergy

240

16.4%

Study too burdensome

202

13.8%

No interest in the study

186

12.6%

No reason

145

9.8%

Telephone screening (n = 572)

  

No HDM allergy

159

27.8%

Low symptom score (<4/12)

158

27.6%

Not interested in study

57

10.0%

Severe asthma

39

6.8%

Language barrier

27

4.7%

Use of immunotherapy in the last 3 years

19

3.3%

Refusing blood sample to be taken

17

3.0%

Age (out of range)

15

2.6%

Allergic complaints <1 year

12

2.1%

History of severe allergic reaction

9

1.6%

Systemic disease

8

1.4%

Use of nasal corticosteroids 1 month before baseline

7

1.2%

Answer forms received after deadline of inclusion period

45

7.9%

Screening visit (n = 249)

  

Only grass pollen or tree pollen sensitization

81

32.5%

No sensitization detectable

75

30.1%

Sensitive to pet at home (confirmed by RAST)

60

24.1%

No informed consent

29

11.7%

Use of unallowed co-medication

4

1.6%