Table 2

Baseline demographic and clinical characteristics of randomised study participants

CharacteristicControl (n=41)PSALTI (n=34)p Value
Age (years)56 (48–67)61 (53–67)0.239
Female, n (%)26 (63)25 (71)0.459
Cough duration (months)48 (24–126)60 (30–126)0.279
FEV1 (L, observed), mean (SD)2.7 (0.9)2.6 (0.7)0.517
FEV1/FVC (%), mean (SD)76 (8.2)76 (5.0)0.686
LCQ, mean(SD)11.9 (3.5)10.4 (3.6)0.073
Cough severity VAS65 (40–83)63 (49–75)0.652
SF-36 PCS,47.1 (41.7–53.6)41.1 (35.6–49.1)0.033*
SF-36 MCS47.7 (38.3–54.9)49.9 (40.5–57.0)0.763
HADS—Anxiety7 (3–10)7 (4–10)0.785
HADS—Depression4 (1–8)5 (2–6)0.620
VPQ17 (11–22)21 (13–27)0.158
CFper hour17.0 (0.4)17.0 (0.4)0.983
C2 (µm)†4.01(0.69)4.74 0.62)0.677
C5 (µm)†9.33 (0.56)8.25 (0.51)0.708
  • Data presented as median (IQR) unless otherwise stated.

  • *p<0.05.

  • †Geometric mean (log SD).

  • C2, capsaicin cough challenge—concentration that resulted in two or more coughs; C5, capsaicin cough challenge—concentration that resulted in five or more coughs; CFper hour, cough frequency per hour over a 24-hour period; HADS, Hospital Anxiety and Depression Scale; LCQ, Leicester Cough Questionnaire; MCS, mental component score; PCS, physical component score; PSALTI, physiotherapy, and speech and language therapy intervention; SF-36, short form 36 questionnaire; VAS, visual analogue scale; VPQ, vocal performance questionnaire.