Content » Vol 95, Issue 3

Clinical Report

Positive Changes in Self-management and Disease Severity Following Climate Therapy in People with Psoriasis

Astrid K. Wahl1, Eva Langeland2, Marie H. Larsen1,3, Hilde S. Robinson1, Richard H. Osborne4 and Anne-Lene Krogstad3

1Department of Health Sciences, Institute of Health and Society, The Medical Faculty, University of Oslo, 2Faculty of Health and Social Sciences, Bergen University College, Bergen, 3Section for Climate Therapy and 5Department of Dermatology, Oslo University Hospital, Oslo, Norway, and 4Population Health Strategic Research Centre, School of Health and Social Development, Deakin University, Melbourne, Australia

The aim of this study was to investigate the impact of climate therapy on self-management in people with psoriasis. This was a prospective study of 254 adults with chronic psoriasis who participated in a 3-week climate therapy (CT) programme. The 8-scale Health Education Impact Questionnaire (heiQ) was completed at baseline, after 3 weeks of CT, and 3 months later. Change was assessed using paired sample t-tests mean (95% confidence interval) change scores (range 1–4). All heiQ scales showed statistically significant improvement after 3 weeks of CT. The greatest improvement was in Health-directed activity, followed by Emotional distress, and Skill and technique acquisition. At the 3-month follow-up, only the Emotional distress scale remained improved. In addition, disease severity (self-administered PASI; SAPASI) improved significantly from before CT to 3 weeks and 3 months after CT. This study suggests that CT provides a range of benefits that are important to people with psoriasis, particularly in the short term. A challenge is how to achieve long-term benefits. Key words: psoriasis; climate therapy; self-management; disease severity.

Accepted Aug 11, 2014; Epub ahead of print Aug 11, 2014

Acta Derm Venereol 2014; XX: XX–XX.

Astrid K. Wahl, Department of Health Sciences, Institute of Health and Society, Forskningsveien 3A, Harald Schjelderups hus, PO Box 1089 Blindern, NO-0317 Oslo, Norway. E-mail: a.k.wahl@medisin.uio.no

Psoriasis affects 2–4% of the population and is probably influenced by genetic, individual and environmental factors (1). Psoriasis may be regarded as a complex long-term condition involving physical, psychological and social challenges (2), including significant impact on daily living (3), functioning and quality of life (4, 5). Psoriasis treatments aim to interrupt the immune-mediated cycle that causes increased production of epidermal cells, thereby reducing inflammation and plaque formation. Psoriasis treatment includes topical medication, ultraviolet (UV) therapy and different kinds of systemic medication. In the Nordic countries, climate therapy (CT) is a publicly funded treatment alternative, among other options for psoriasis. Every year, approxi­mately 500 Norwegians with psoriasis attend CT on Gran Canaria in the Canary Islands, Spain. The 3-week treatment programme includes individualized scheduled sun exposure, daily physical training, education about psoriasis, comorbidity and treatments, group discussions, psychosocial support and medical consultations. CT has been shown to reduce Psoriasis Area and Severity Index (PASI) by 75% (6), inter alia due to the sun-induced reduction in immune activity in psoriasis lesions (7, 8). The therapy also increases the serum levels of vitamin D and reduces lipids (9). Because the CT programme includes education and support, it is reasonable to think that such a programme could also improve self-management as well as disease severity.

Self-management has emerged as a critical aspect of care for individuals with a long-term illness (10–12). The core of self-management is that people actively participate in maintaining and promoting their own health and care (10). Only a small number of studies have evaluated self-management interventions in psoriasis. De Korte et al. (13) reported that psoriasis patients participating in a disease management intervention had reduced disease severity, improved adherence to treatment regimens, and improved quality of life, and reported a high degree of satisfaction with the intervention. Pagliarello et al. (14) found that an educational intervention for psoriasis patients increased their empowerment and knowledge about the disease. Ersser et al. (15) suggested that tailored education could improve adherence and self-management. A recently published systematic literature review showed that little evidence is available to support the effects of educational and self-management interventions in patients with psoriasis. Compared with other chronic conditions, there appear to be few effective disease-specific tailored educational programmes for psoriasis (16). Hence, the aim of this study was to evaluate self-management and disease severity over a period of 4 months following CT in patients with psoriasis.

METHODS

Study design and population

The present study was a pre–post study of Norwegian adults with psoriasis who participated in CT for 3 weeks on Gran Canaria, located in the Atlantic Ocean at 28°N, 16°W. The study was conducted from April 2009 to January 2010. To be qualified for CT, the patient’s PASI score must be above 7. Applications were evaluated by a dermatologist at the Section for Climate Therapy at Oslo University Hospital. Eligible patients were informed about the study after arrival at the CT centre. Seventy-four percent of the patients consented to participate. The inclusion criterion was age 20–80 years, and the exclusion criterion was concomitant use of systemic anti-psoriatic medication.

Questionnaires were administered at the start (T1), directly after 3 weeks of therapy (T2) and 3 months after T2 (T3). Data were available for 254, 251 and 207 respondents, respectively.

Ethical approval

The study was approved by the Oslo University Hospital and Norwegian Social Science Data Services, and recommended by the Regional Committee for Medical Research Ethics for Southern Norway. The study was carried out in accordance with the Declaration of Helsinki.

Climate therapy programme (CT)

Sun therapy was scheduled individually with respect to skin type and UV index (6). Patients received, a mean of 250 standard erythema doses (SED) (6). They were examined at arrival, after one week and 3 weeks. The teaching programme comprised lectures and dialogues about psoriasis pathogenesis, manifestations, comorbidity, quality of life, and treatment options. The importance of a healthy lifestyle was stressed, with focus on physical activity, stress reduction and healthy eating. Small group discussions focused on ways to manage psoriasis in daily life (Fig. 1).

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Fig. 1. Aim and content of climate therapy programme.

The centre is administered from the University Hospital in Oslo (Section for CT). A full-time employed dermatologist, 4 nurses (with 5–30 years experience from CT), and a physiotherapist (with 15 years’ experience in rehabilitation) monitored the patients and provided individual and group-based education, guidance and daily training. During the last 10 years this CT concept has been successively developed in accordance with the increased holistic comprehension of the disease. Research projects at the centre and educational methods/techniques have successively been introduced and supervised from a team of specialists at Oslo University Hospital/Oslo University and incorporated to continuously improve the programme.

Measures

Sociodemographic and clinical variables. Sociodemographic variables, such as age, sex, cohabitation, employment status, and level of formal education, were assessed. Clinical variables included the duration of psoriasis, comorbidity, previous CT, and disease severity, the latter being measured by the self-administered PASI (SAPASI) (17).

Self-management assessment: Health Education Impact Questionnaire (heiQ™). The heiQ provides a comprehensive evaluation of patient education programmes (12). It is widely used and is available in many languages (18). It was developed through extensive stakeholder engagement, including nominal group techniques, to ensure its relevance to patients, practitioners and policymakers across settings (12, 19). The heiQ comprises 40 items across 8 independent scales: Health-directed activity, Positive and active engagement in life, Self-monitoring and insight, Constructive attitudes and approaches, Skill and technique acquisition, Social integration and support, Health service navigation, and Emotional distress (a reversed scale). Table SI1 gives a description of each scale. Each of the 8 scales has 4–7 items that are rated on a 4-point scale, where 1 = strongly disagree, 2 = disagree, 3 = agree, and 4 = strongly agree. The items in each scale are summed, and the sum is divided by its number of items. Hence, the scale scores range between 1 and 4. A higher score indicates better self-management, except for the Emotional distress scale, which is reversed. Results from psychometric studies of the heiQ show satisfactory results across diverse settings (18, 20–22). The heiQ was translated and adopted into Norwegian using the guidelines of Hawkins & Osborne (23). Cronbachs’ alpha for the individual scales are shown in Table SI1.

Statistical analyses

Statistical analyses were conducted using SPSS (version 19.0). Descriptive analyses were performed to assess the frequency, mean, standard deviation (SD), and minimum and maximum scores. Cronbach’s alpha was used to estimate the internal consistency of the scale (reliability). Paired-sampled t-tests were used to evaluate the changes from baseline to follow-up, and 95% confidence intervals (CIs) were calculated. A small amount of missing data was identified across the heiQ scales. Data from individuals with ≥ 10% missing data were eliminated. The questionnaire data from individuals with <10% of missing data were replaced using the SPSS EM procedure (IBM Cons., New York, NY).

RESULTS

Characteristics of the sample

The mean (SD) age of the respondents was 47 (12) years (range 20–80 years). One hundred and two (40%) were women, and 153 (60%) had 12 years of education; 70 (28%) reported living alone. The mean (SD) disease duration was 24 (13) years (range 1–60 years). The mean (SD) pre-treatment disease severity (SAPASI) score was 8.6 (6.2), and 111 (44%) reported comorbidity (see Table SII1).

Changes in SAPASI scores

The disease severity (SAPASI score) improved significantly, from 8.6 (95% CI: 7.7–9.4) at T1 to 1.6 (1.2–2.1) at T2 (p < 0.001). At T3 the SAPASI score was 6.4 (5.7–7.2), which is also a significant improvement compared with T1 (p < 0.001).

Changes in heiQ scales

There was significant improvement in all heiQ scales from baseline (T1) to immediately after CT (T2) (p < 0.001) (see Table I). The largest mean (95% CI) improvements were for Health-directed activity 0.32 (0.25–0.40), followed by Emotional distress –0.22 (–0.30 to –0.16) and Skill and technique acquisition 0.22 (0.16–0.27).

Three months after CT (T3), the Emotional distress scale was the only scale which showed significant improvement compared with baseline (T1) mean change (95% CI) –0.11 (–0.19 to –0.03). In the scales Health service navigation and Positive and active engagement in life the mean scores were significantly worse compared with the baseline scores (T1). For further information on changes, see Table I.

Table I. Self-management outcomes for people with psoriasis

Baseline to 3-week follow-up (n = 251)

Baseline to 3-month follow-up (n = 207)

heiQ scales

Baselinea

Follow-upa

Change from baseline

95% CI of mean change

p-value

Baselinea

Follow-upa

Change from baseline

95 % CI of mean change

p-value

1. Positive & active engagement in life

3.23

3.36

0.13

0.08–0.17

< 0.001

3.24

3.16

–0.08

–0.14 to –0.03

0.002

2. Health-directed activity

2.96

3.28

0.32

0.25–0.40

< 0.001

3.02

3.00

–0.02

–0.09–0.06

0.72

3. Skill and technique acquisition

2.78

3.00

0.22

0.16–0.27

< 0.001

2.80

2.87

0.07

0.00–0.14

0.06

4. Constructive attitudes and approaches

3.15

3.29

0.14

0.09–0.19

< 0.001

3.18

3.13

–0.05

–0.11–0.01

0.16

5. Self-monitoring and insight

3.04

3.17

0.13

0.09–0.18

< 0.001

3.06

3.07

0.01

–0.04–0.07

0.56

6. Health service navigation

3.04

3.14

0.10

0.03–0.14

< 0.001

3.06

2.96

–0.10

–0.16 to –0.04

0.001

7. Social integration and support

2.94

3.09

0.15

0.09–0.21

0.001

2.97

2.92

–0.05

–0.12–0.02

0.15

8. Emotional distressb

2.22

2.00

–0.22

–0.30 to –0.16

< 0.001

2.21

2.10

–0.11

–0.19 to –0.03

0.004

aMean values. bReversed scale (low = good). heiQ: Health Education Impact Questionnaire.

DISCUSSION

This study shows that self-management improved significantly from before to immediately after CT. The greatest improvements were seen in Health-directed activity, followed by Emotional distress and Skill and technique acquisition. However, after 3 months, only Emotional distress and disease severity remained significantly improved compared with the baseline score. Hence, long-lasting changes in self-management in relation to CT may be questioned. Similar positive short-term results with regard to improved quality of life have previously been reported (24). Returning to everyday life after CT may be associated with reduced access to healthcare professionals and lack of support from peers compared with those received during the CT programme. Post-CT booster interventions at home may be an option to prolong the positive changes following CT.

With regard to self-management the largest improvement were observed for Health-directed activity and Skill and technique acquisition, especially immediately after the intervention. In addition to sun exposure, the CT programme includes health education, physical activity, and a healthy diet (see Fig. 1). Accordingly, the improvements in Health-directed activity and Skill and technique acquisition are consistent with the content of the intervention. In a recent study of the present sample, psoriasis-related knowledge was measured using the Psoriasis Knowledge Questionnaire, and significant short- and long-term improvements were noted (25). It is known that health-related knowledge is important (26), although not sufficient by itself to provide motivation to change to a healthier lifestyle pattern (27, 28). Thus, it is important to understand how to translate this knowledge into promoting health in everyday life.

Emotional distress was the only self-management scale that remained improved 3 months after CT. Psychological distress (29, 30), higher levels of anxiety, depression, worry and suicide ideation have been reported as common problems in people with psoriasis compared with controls (31). The different components of the CT programme, such as the relaxing environment, support from other patients and healthcare personnel, may have contributed to an immediate positive outlook on life, which in turn, may have influenced the patients’ perceptions of emotional well-being. Furthermore, reduced disease severity and symptom burden (e.g. skin discomfort, itch and pain) following CT certainly may play a major role in reducing the level of emotional distress.

One may raise the question whether all of the self-management areas reflected in the heiQ scales are equally important and relevant for measuring outcomes of CT, since the CT programme is closely linked to reduction in disease severity, and to increase knowledge and insight specific to psoriasis. Hence, the focus on heiQ scales, such as Self-monitoring and insight, Skill and technique acquisition and Health-directed activity seem specifically important.

Self-assessed disease severity, measured by SAPASI, was significantly improved both immediately after CT and 3 months after, compared with before CT. The immediate improvement in disease severity after CT has been shown in several previous studies (e.g. 6). Although the improvement was reduced at 3 months after CT, it was still significant. The reason for the prolonged effect may be that more effort has been made to include systematic health education during CT, which in turn may have increased knowledge and insight regarding the importance of adherence to treatment.

Although the results of this study seem promising, the absence of a control group means that full attribution of improvements after CT is not possible, because we cannot exclude a range of biases (32, 33). Further research should use a stronger study design, such as controlled trial to strengthen the evidence for both the short- and long-term effects of CT on outcomes, such as self-management. The implementation of such controlled trials is a challenge in settings where an intervention has become integrated into routine practice. This is the first study reporting data on the Norwegian version of the heiQ. The translation and adaptation procedure followed well-established principles for cross-culture translation and adaption of questionnaires. The results from our study may indicate good internal consistency, with alpha range from 0.7 to 0.9 across the heiQ scales, and responsiveness in the context of CT and psoriasis.

Conclusion

This study suggests that CT provides a range of benefits that are important to people with psoriasis, particularly in the short term. However, one may question how to achieve long-term benefits. Implementation and evaluation of post-CT self-management interventions may expand our understanding of its effectiveness. With regard to the practical implications, this study highlights the importance of considering the content of the self-management intervention and in which domains CT should generate benefits. Alongside this, further work is required to ensure self-management interventions seeking to maximize benefits over the long term.

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1http://www.medicaljournals.se/acta/content/?doi=10.2340/00015555-1939

REFERENCES

1. Parisi R, Symmons DPM, Griffiths CEM, Ashcroft DM, IMPACT project team. Global epidemiology of psoriasis: a systematic review of incidence and prevalence. J Invest Dermatol 2012; 133: 377–385.

2. Nelson PA, Chew-Graham CA, Griffiths CEM, Cordingley L, on behalf of the IMPACT team. Recognition of need in health care consultations: a qualitative study of people with psoriasis. Br J Dermatol 2012; 168: 354–361.

3. Stern RS, Nijsten T, Feldman SR, Margolis DJ, Rolstad T. Psoriasis is common, carries a substantial burden even when not extensive, and is associated with widespread treatment dissatisfaction. J Investig Dermatol Symp Proc 2004; 9: 136–139.

4. Linder D, Dall’Olio E, Gisondi P, Berardesca E, De Gennaro E, Pennella AG, et al. Perception of disease and doctor-patient relationship experienced by patients with psoriasis. Am J Clin Dermatol 2009; 10: 325–330.

5. Bewley A, Page B. Maximizing patient adherence for optimal outcomes in psoriasis. J Eur Acad Dermatol Venereol 2011; 25: 9–14.

6. Nilsen LT, Søyland E, Krogstad AL. Estimated ultraviolet doses to psoriasis patients during climate therapy. Photodermatol Photoimmunol Photomed 2009; 25: 202–208.

7. Heier I, Søyland E, Krogstad AL, Rodríguez-Gallego C, Nenseter MS, Jahnsen FL. Sun exposure rapidly reduces plasmacytoid dendritic cells and inflammatory dermal dendritic cells in psoriatic skin. Br J Dermatol 2011; 165: 792–801.

8. Søyland E, Heier I, Rodríguez-Gallego C, Mollnes TE, Johansen FE, Holven KB, et al. Sun exposure induces rapid immunological changes in skin and peripheral blood in patients with psoriasis. Br J Dermatol 2011; 164: 344–355.

9. Osmancevic A, Nilsen LT, Landin-Wilhelmsen K, Søyland E, Abusdal Torjesen P, et al. Effect of climate therapy at Gran Canaria on vitamin D production, blood glucose and lipids in patients with psoriasis. J Eur Acad Dermatol Venereol 2009; 23: 1133–1140.

10. Von Korff M, Glasgow RE, Sharpe M. Organising care for chronic illness. BMJ 2002; 325: 92–94.

11. Osborne RH, Wilson T, Lorig KR, McColl GJ. Does self-management lead to sustainable health benefits in people with arthritis? A 2-year transition study of 452 Australians. J Rheumatol 2007; 34: 1112–1117.

12. Osborne RH, Elsworth GR, Whitfield K. The Health Education Impact Questionnaire (heiQ): an outcomes and evaluation measure for patient education and self-management interventions for people with chronic conditions. Patient Educ Couns 2007; 66: 192–201.

13. De Korte J, Van Onselen J, Kownacki S, Sprangers MAG, Bos JD. Quality of life in patients with psoriasis: an initial clinical study of an international disease management programme. J Eur Acad Dermatol Venereol 2005; 19: 35–41.

14. Pagliarello C, Calza A, Armani E, Di Pietro C, Tabolli S. Effectiveness of an empowerment- based intervention for psoriasis among patients attending a medical spa. Eur J Dermatol 2011; 21: 62–66.

15. Ersser SJ, Cowdell FC, Latter SM, Healy E. Self-management experiences in adults with mild–moderate psoriasis: an exploratory study and implications for improved support. Br J Dermatol 2010; 163: 1044–1049.

16. Larsen MH, Hagen KB, Krogstad AL, Aas E, Wahl AK. Limited evidence of the effects of patient education and self-management interventions in psoriasis patients: a systematic review. Patient Educ Couns 2014; 94: 158–169.

17. Feldman SR, Fleischer AB Jr, Reboussin DM, Rapp SR, Exum ML, Clark AR, Nurre L. The self-administered psoriasis area and severity index is valid and reliable. J Invest Dermatol 1996; 106: 183–186.

18. Osborne RH, Batterham R, Livingston J. The evaluation of chronic disease self-management support across settings: the international experience of the Health Education Impact Questionnaire Quality Monitoring System. Nurs Clin North Am 2011; 46: 255–270.

19. Nolte S, Elsworth GR, Sinclair AJ, Osborne R. The extent and breadth of benefits from participating in chronic disease self-management courses: a national patient reported outcomes survey. Patient Educ Couns 2007; 65: 351–360.

20. Schuler M, Musekamp G, Faller H, Ehlebracht-König I, Gutenbrunner C, Kirchhof R, et al. Assessment of proximal outcomes of self-management programs: translation and psychometric evaluation of a German version of the Health Education Impact Questionnaire (heiQ). Qual Life Res 2012; 22: 1391–1403.

21. Morita R, Arakida M, Osborne RH, Nolte S, Elsworth GR, Mikami H. Adaptation and validation of the Japanese version of the Health Education Impact Questionnaire (heiQ-J) for the evaluation of self-management education interventions. Jpn J Nurs Sci 2013; 10: 255–266.

22. Nolte S, Elsworth GR, Sinclair AJ, Osborne, R. The inclusion of ‘then-test’ questions in post-test questionnaires alters post-test responses: a randomized study of bias in health program evaluation. Qual Life Res 2012; 21: 487–494.

23. Hawkins M, Osborne RH. Questionnaire translation and cultural adaptation procedure. Melbourne: Centre for Rheumatic Diseases, Department of Medicine, Royal Melbourne Hospital and University of Melbourne, Australia; 2007.

24. Wahl AK, Mørk C, Cooper BA, Padilla G. No long-term changes in psoriasis severity and quality of life following climate therapy. J Am Acad Dermatol 2005; 52: 699–701.

25. Wahl AK, Moum T, Robinson HS, Langeland E, Larsen MH, Krogstad AL. Psoriasis patients’ knowledge about the disease and treatments. Dermatol Res Pract 2013; 2013: 921737.

26. Renzi C, Di Pietro C, Tabolli S. Participation, satisfaction and knowledge level of patients with cutaneous psoriasis or psoriatic arthritis. Clin Exp Dermatol 2011; 36: 885–888.

27. Bodenheimer T. Helping patients improve their health-related behaviors: what system changes do we need? Dis Manag 2005; 8: 319–330.

28. Lorig K, Holman H. Self-management education: history, definition, outcomes, and mechanisms. Ann Behav Med 2003; 26: 1–7.

29. Kirby B, Richards HL, Mason DL, Fortune DG, Main CJ, Griffiths CEM. Alcohol consumption and psychological distress in patients with psoriasis. Br J Dermatol 2008; 158: 138–140.

30. Kossakowska MM, Cieścińska C, Jaszewska J, Placek WJ. Control of negative emotions and its implication for illness perception among psoriasis and vitiligo patients. J Eur Acad Dermatol Venereol 2010; 24: 429–433.

31. Griffiths CE, Richards HL. Psychological influences in psoriasis. Clin Exp Dermatol 2001; 26: 338–342.

32. Buchbinder R, Kalmes DF. Vertebroplasty: when randomized placebo-controlled trials results clash with common belief. Spine J 2010; 10: 241–343.

33. Carragee EJ. The vertebroplasty affair: the mysterious case of the disappearing effect size. Spine J 2010; 10: 191–192.

Supplementary content
Table SI
Table SII