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Visiting a sauna: does inhaling hot dry air reduce common cold symptoms? A randomised controlled trial

Daniel Pach, Bettina Knöchel, Rainer Lüdtke, Katja Wruck, Stefan N Willich and Claudia M Witt
Med J Aust 2010; 193 (11): 730-734. || doi: 10.5694/j.1326-5377.2010.tb04127.x
Published online: 6 December 2010

Abstract

Objective:

Design, setting and participants: A randomised single-blind controlled trial with a treatment duration of 3 days and a follow-up period of 4 days was conducted at a sauna in Berlin, Germany. Between November 2007 and March 2008 and between September 2008 and April 2009, 157 patients with symptoms of the common cold were randomly assigned to an intervention group (n = 80) and a control group (n = 77).

Interventions: Participants in the intervention group inhaled hot dry air within a hot sauna, dressed in a winter coat, whereas participants in the control group inhaled dry air at room temperature within a hot sauna, also dressed in a winter coat.

Main outcome measures: Area under the curve (AUC) summarising symptom severity over time (Days 2, 3, 5 and 7), symptom severity scores for individual days, intake of medication for the common cold and general ill feeling.

Results: No significant difference between groups was observed for AUC representing symptom severity over time (intervention group mean, 31.2 [SEM, 1.8]; control group mean, 35.1 [SEM, 2.3]; group difference, 3.9 [95% CI, 9.7 to 1.9]; P = 0.19). However, significant differences between groups were found for medication use on Day 1 (P = 0.01), symptom severity score on Day 2 (P = 0.04), and participants’ ratings of the effectiveness of the therapy on Day 7 (P = 0.03).

Conclusion: Inhaling hot air while in a sauna has no significant impact on overall symptom severity of the common cold.

Trial registration: ClinicalTrials.gov identifier NCT00552981.

The common cold, mainly caused by rhinoviruses or coronaviruses,1,2 is a frequent problem all over the world. Although the symptoms are generally benign, viral colds result in significant costs to the economy due to lost workdays and school attendance.3 Convincing treatment options without side effects are not known.4 Traditionally, the local application of heat is used to treat the symptoms of the common cold — for example, ingesting hot fluids such as tea or chicken soup,5 or inhaling hot vapour.6 Moreover, few clinical trials have been conducted to evaluate such treatment options.6-8 It has been suggested that local hyperthermia of the nasal mucosa can affect rhinovirus replication.7-9 A Cochrane review of six trials — one from Israel, two from the United Kingdom, and three from the United States — found that only the studies from Israel and UK showed that steam was beneficial for relief of common cold symptoms.6 Results on symptom indices were equivocal; therefore, it was concluded that steam inhalation cannot be recommended for the routine treatment of common cold symptoms and further blind randomised controlled trials needed to be conducted.

In the German city of Essen, a sauna with dry air heated to 90°C exists (www.unperfekthaus.de/projekte/angezogen-sauna) where people can visit dressed in street clothes for the relief of common cold symptoms. This type of sauna is widely available and offers enough dry air to heat the throat, and wetness of the skin is only caused by sweating, not by high humidity. With the aim of heating the throat, people stay in this sauna for only a short period to avoid sweating. Use of this type of sauna has little in common with that of a regular sauna, where one usually stays longer than 10 minutes and sweating is desired. If proven to be effective, a dry air sauna would be an interesting option for treating common cold symptoms.

On the basis of experiences with the sauna in Essen, the aim of our study was to test the hypothesis that inhaling hot dry air reduces common cold symptoms. To do this, we compared the efficacy of applying hot dry air versus dry air at room temperature to the throat of patients with a newly acquired common cold, using a symptom severity score.

Methods
Results
Participants

Of 287 people who expressed interest in the study, 157 were randomly assigned to the intervention or control arms of the study (intervention group: n = 80, control group: n = 77; Box 2). The mean age of these participants was 32.0 years (SD, 10.2 years; median, 28 years), and 93 participants (59.2%) were women. Mean age and body mass index differed significantly between groups (P = 0.03 and P = 0.003, respectively) but other baseline characteristics were comparable (Box 3).

Discussion

Participants who had inhaled hot air in the sauna did not show significantly different common cold symptoms compared with participants who had inhaled air at room temperature.

The main strengths of this trial are the rigorous study design, large sample size, high compliance and follow-up rates, and the clear research hypothesis. Moreover, the sauna set-up was very similar for the intervention and control groups, and the groups were comparable at baseline.

We might have underestimated the effect of sitting in the sauna. For example, some participants experienced pleasant warming of the face and relaxation while sitting in the sauna and less headache afterwards. The warm feeling in a sauna during a cold might have more impact on symptoms than inhaling hot air, resulting in similar treatment outcomes in both groups. If so, we might have chosen the wrong research hypothesis.

A short stimulus of 3 minutes was used to avoid sweating and drying of the mucus in the throat. The duration of each sauna stay in our study may have been too short, and the sauna stays may not have been frequent enough to cause a substantial effect. Also, blinding for the air temperature was difficult. In addition, the outcome measures we used were based only on participants’ reports. We did not include any objective outcome measures, such as plasma cytokine levels10,11 or nasal airflow resistance.5

Participants in our study started with a severity score of about 9 and reached a score of about 3 on Day 7. This course of disease is comparable with results from placebo groups in studies used to evaluate the efficacy of zinc acetate.10,11 After enrolment in the study, the severity score lowered without the initial worsening of symptoms that one would expect within the first 48 hours of a common cold.12 Perhaps the peak of symptom severity had already been reached. However, initial worsening is often only observable in studies where participants suffer from an experimentally induced common cold.13 Taking this lack of initial worsening as an indication of longer disease duration (ie, greater than 24 hours at the start of the study), our intervention might have been too late to have had an impact on the course of the disease. However, the context effect14 or placebo effect15,16 may explain the initial improvement of symptoms. The placebo effect may also explain the significant group differences for the participants’ ratings of symptom severity on Day 2, medication intake on Day 1, and ratings of the effectiveness of the therapy on Day 7. As more participants in the control group guessed correctly that they were in the control group, the placebo effect might have been higher in the intervention group. Although we used dry air to heat the throat, instead of humidified air in the nose as done in most studies evaluated in the Cochrane review,6 we support the view that steam inhalation cannot yet be recommended for the routine treatment of common cold symptoms.

Inhaling hot dry air while in a sauna does not have a significant impact on the symptom severity of a common cold.

3 Baseline characteristics of study participants

Intervention (n = 80)


Control (n = 77)


P

Mean (SD) or no. (%)

Median

Mean (SD) or no. (%)

Median


Women

46 (58%)

47 (61%)

0.65

Age (years)

33.7 (10.8)

30.0

30.2 (9.4)

27.0

0.03

Body mass index (kg/m2)

23.4 (4.0)

22.8

21.8 (2.9)

21.3

0.003

No. of common colds in past 6 months

0.9 (1.1)

1

1.1 (1.5)

1

0.63

Duration of symptoms (h)

19.0 (6.1)

21.5

18.3 (5.9)

19.0

0.44

Symptom severity score

Total

9.4 (4.0)

9

9.1 (3.1)

9

0.92

Cough

0.9 (0.7)

1

0.8 (0.8)

1

0.24

Headache

1.1 (0.9)

1

1.2 (1.0)

1

0.47

Hoarseness

0.8 (0.8)

1

0.7 (0.8)

0

0.20

Muscle ache

0.6 (0.8)

0

0.7 (0.7)

1

0.33

Nasal drainage

1.5 (0.9)

2

1.5 (0.9)

2

0.84

Nasal congestion

1.1 (0.9)

1

1.2 (0.9)

1

0.65

Scratchy throat

1.3 (0.9)

1

1.4 (0.7)

1

0.52

Sore throat

1.1 (0.9)

1

1.0 (0.9)

1

0.30

Sneezing

0.9 (0.8)

1

0.8 (0.8)

1

0.69

Fever

0.2 (0.4)

0

0.1 (0.3)

0

0.01

General ill feeling*

3.8 (1.7)

3

4.2 (1.6)

4

0.08

Use of medications for other diseases

15 (19%)

24 (31%)

0.07

Use of medications for common cold

15 (19%)

14 (18%)

0.93

Consultation because of common cold

0

1 (1%)

Expected outcome

0.70

Recovery

2 (3%)

7 (9%)

Distinct improvement

37 (46%)

31 (40%)

Light improvement

41 (51%)

38 (49%)

No improvement

0

1 (1%)

Expected effectiveness

0.46

Very effective

7 (9%)

12 (16%)

Effective

55 (69%)

48 (62%)

Small effect

18 (23%)

17 (22%)

No effect

0

0


* On a scale of 0 to 10 (0 = completely healthy; 10 = very ill). Before the beginning of the study, during present common cold.

4 Outcome measures for the intention-to-treat population

Intervention (n = 79)


Control (n = 76)


Mean ± SEM
(95% CI)*

Mean ± SEM
(95% CI)*

Group difference
(95% CI)*

P*


Area under the curve for symptom severity on Days 2, 3, 5 and 7

31.2 ± 1.8 (27.6 to 34.8)

35.1 ± 2.3 (30.5 to 39.7)

3.9 ( 9.7 to 1.9)

0.19

Symptom severity score

Day 1

6.7 ± 0.3 (6.1 to 7.3)

6.5 ± 0.2 (6.1 to 7.0)

0.2 ( 0.6 to 0.9)

0.69

Day 2

6.5 ± 0.3 (5.9 to 7.2)

7.6 ± 0.4 (6.9 to 8.3)

1.0 ( 2.0 to 0.1)

0.04

Day 3

5.5 ± 0.4 (4.7 to 6.2)

6.5 ± 0.5 (5.5 to 7.4)

1.0 ( 2.2 to 0.2)

0.11

Day 5

5.0 ± 0.4 (4.2 to 5.8)

5.4 ± 0.5 (4.4 to 6.5)

0.5 ( 1.8 to 0.8)

0.47

Day 7

3.1 ± 0.4 (2.4 to 3.8)

3.6 ± 0.5 (2.7 to 4.5)

0.5 ( 1.6 to 0.6)

0.40


Percentage (95% CI)*

Percentage (95% CI)*

Odds ratio (95% CI)*

P*


Proportion of participants who took medication for common cold

Day 1

3% (1% to 9%)

15% (8% to 28%)

0.2% (0.04% to 0.7%) 

0.01

Day 2

6% (2% to 16%)

9% (5% to 18%)

0.6% (0.2% to 2%)

0.47

Day 3

9% (4% to 18%)

12% (5% to 23%)

0.7% (0.2% to 2%)

0.56

Day 4

9% (4% to 19%)

12% (6% to 24%)

0.7% (0.2% to 2%)

0.51

Day 5

10% (5% to 21%)

9% (4% to 20%)

1% (0.3% to 4%)

0.85

Day 6

7% (3% to 16%)

7% (3% to 17%)

1% (0.3% to 4%)

0.94

Day 7

5% (2% to 14%)

8% (3% to 18%)

0.7% (0.2% to 3%)

0.56


No. (%)

No. (%)

P


Participant’s rating of outcome on Day 7

0.56

Recovery

3 (4%)

3 (4%)

Distinct improvement

13 (16%)

9 (12%)

Light improvement

43 (54%)

37 (49%)

No improvement

20 (25%)

27 (35%)

Participant’s rating of effectiveness on Day 7

0.03

Very effective

2 (3%)

1 (1%)

Effective

30 (38%)

22 (29%)

Small effect

41 (52%)

32 (42%)

No effect

6 (8%)

21 (28%)

Participant’s guess of group allocation on Day 3§

< 0.001

Intervention

41 (52%)

14 (18%)

Control

37 (47%)

63 (82%)


* Data were adjusted using a generalised estimation equation model. Odds ratio < 1 indicates less medication use in intervention group. From Days 1 to 7. § Data missing for one participant in the intervention group on Day 3 (n = 79 for intervention group, n = 77 for control group).

  • Daniel Pach1
  • Bettina Knöchel1
  • Rainer Lüdtke2
  • Katja Wruck1
  • Stefan N Willich1
  • Claudia M Witt1

  • 1 Institute for Social Medicine, Epidemiology and Health Economics, Charité University Medical Center, Berlin, Germany.
  • 2 Karl und Veronica Carstens Foundation, Essen, Germany.


Correspondence: daniel.pach@charite.de

Acknowledgements: 

We thank Beatrice Eden and Iris Bartsch for their support with daily patient management, and Reinhard Wiesemann who developed the idea for this setting and provided the sauna cabin.

Competing interests:

The study was funded by the Karl und Veronica Carstens Foundation.

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