https://doi.org/10.4081/ripppo.2021.486
The indirect effect of a focus group for psoriatic patients on their caregivers
Submitted: August 1, 2020
Accepted: December 29, 2020
Published: March 30, 2021
Accepted: December 29, 2020
Abstract Views: 12551
PDF: 429
HTML: 21
HTML: 21
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Psoriasis is a chronic skin disease involving not only epidermic damages but also psychological distress for patients and their family caregivers. Little is known about the effects of a psychological support for psoriatic patients on their caregivers’ well-being. The goal of the present study was to investigate the indirect effects of the participation in a dynamic focus group reserved for psoriatic patients on their caregivers in terms of quality of life. The study involved 52 psoriatic patients and 41 family caregivers. Patients’ wellbeing was assessed using the dermatology quality of life index, hospital anxiety and depression scale. The impact of the disease on caregivers was assessed using the family dermatology life quality index (FDLQI). Data were analyzed with linear mixed models. The caregivers of psoriatic patients involved in the psychodynamic focus group reported levels of FDLQI that decreased over time, therefore showing an improvement in their quality of life in relation to the pathology of their relatives; the caregivers of patients who did not participate in the psychodynamic focus group, instead, had levels of FDLQI that were stable over time. The results provide preliminary evidence that the group setting of the Psychodynamic Focus Group may alleviate the negative impact of psychosomatic disease on the caregivers.
Anzieu, D. (1993). L’Io-pelle familiare e gruppale. Interazioni, 7, 9-17.
Ak, M., Haciomeroglu, B., Turan, Y., Lapsekili, N., Doruk, A., Bozkurt, A., & Akar, A. (2012). Temperament and character properties of male psoriasis patients. Journal of Health Psychology, 17(5), 774-781.
DOI: https://doi.org/10.1177/1359105311423863
Baranzoni, N., Scalone, L., Mantovani, LG., De Portu, S., Monzini, MS., & Giannetti, A. (2007). Validazione della versione Italiana dell’Indice Dermatologico della Qualità di Vita. Giornale Italiano di Dermatologia e Venereologia, 142(3), 209-214.
Basra, M. K., Fenech, R., Gatt, R. M., Salek, M. S., & Finlay, A. Y. (2008). The dermatology life quality index: a comprehensive review of validation data and clinical results. British Journal of Dermatology, 159(5), 997-1035. https://doi.org/10.1111/j.1365-2133.2008.08832.x
DOI: https://doi.org/10.1111/j.1365-2133.2008.08832.x
Basra, M. K., & Finlay, A.Y. (2007). The family impact of skin diseases: the greater patient concept. British Journal of Dermatology, 156(5), 929-937.
DOI: https://doi.org/10.1111/j.1365-2133.2007.07794.x
Bundy, C., Pinder, B., Bucci, S., Reeves, D., Griffiths, CE., & Tarrier, N. (2013). A novel, web-based, psychological intervention for people with psoriasis: the electronic Targeted Intervention for Psoriasis (eTIPs) study. British Journal of Dermatology, 169, 329-336.
DOI: https://doi.org/10.1111/bjd.12350
Chamoun, A., Goudetsidis, L., Poot, F., Bourdeaud’hui, F., & Titeca, G. (2015). Psoriasis and depression. Revue Medicale de Bruxelles, 36(1), 23-28.
Connor, CJ., Liu, V., & Fiedorowicz, JG. (2015). Exploring the physiological link between psoriasis and mood disorders. Dermatology Research Practice, 15, 1-12.
DOI: https://doi.org/10.1155/2015/409637
Costantini, M., Musso, M., Viterbori, P. , Bonci, F., Del Mastro, L., Garrone, O., Venturini, M. & Morasso, G. (1999). Detecting psychological distress in cancer patients: validity of the Italian version of the hospital anxiety and depression scale. Support Care Cancer, 7(3), 121-127.
DOI: https://doi.org/10.1007/s005200050241
Del-Pino-Casado, R., Frías-Osuna, A., Palomino-Moral, P. A., Ruzafa-Martínez, M., & Ramos-Morcillo, A. J. (2018). Social support and subjective burden in caregivers of adults and older adults: a meta-analysis. PLoS One, 13(1): e0189874.
Eghlileb, A. M., Davies, E. E., & Finlay, A. Y. (2007). Psoriasis has a major secondary impact on the lives of family members and partners. British Journal of Dermatology, 156(6), 1245-1250.
DOI: https://doi.org/10.1111/j.1365-2133.2007.07881.x
Fabbrini, G., Abbruzzese, G., Barone, P., Antonini, A., Tinazzi, M., Castegnaro, G., Rizzoli, S., Morisky, D. E., Lessi, P.,& Ceravolo, R. (2013). Adherence to anti-Parkinson drug therapy in the ‘‘REASON’’ sample of Italian patients with Parkinson’s disease: the linguistic validation of the Italian version of the ‘Morisky Medical Adherence scale-8 items’; On behalf of the REASON study group. Neurology Science, 34, 2015-2022.
DOI: https://doi.org/10.1007/s10072-013-1438-1
Feldman, S. R., Fleischer, A. B., Reboussin, D. M., Rapp, S. R., Exum, M. L., Clark, A. R., & Nurre, L. (1996). The self-administered psoriasis area and severity index is valid and reliable. Journal of Investigation in Dermatology, 106, 83-86.
DOI: https://doi.org/10.1111/1523-1747.ep12329912
Finlay, A.Y., & Khan, G.K. (1994). Dermatology life quality index (DLQI)--a simple practical measure for routine clinical use. Clinical and Experimental Dermatology 19 (3), 210-216.
DOI: https://doi.org/10.1111/j.1365-2230.1994.tb01167.x
Fortune, D., Richards, H. L., Main, C. J., & Griffiths, C. E. (2000). Pathological worrying, illness perceptions and disease severity in patients with psoriasis. British Journal of Health Psychology, 5(1), 71-82.
DOI: https://doi.org/10.1348/135910700168775
Goldberg, A. R., & Rickler, S. R. (2011). The role of family caregiver for people with chronic illness. Medicine and Health (Rhode Island), 94(2), 41-42.
Grapsa, E., Pantelias, K., Ntenta, E., Pipili, C., Kiousi, E., Samartzi, M., Karagiannis, S., & Heras. P. (2014). Caregivers’ experience in patients with chronic diseases. Social Work in Health Care, 53(7), 670-678.
DOI: https://doi.org/10.1080/00981389.2014.925998
Haley, J., & Hoffman, L. (1967). Techniques of family therapy. New York, NY: Basic Books.
Kabat-Zinn, J., Wheeler, E., Light, T., Skillings, A., Scharf, M. J., Cropley, T. G., Hosmer, D., & Bernhard, J. D. (1998). Influence of a mindfulness meditation based stress reduction intervention on rates of skin clearing in patients with moderate to severe psoriasis undergoing phototherapy (UVB) and photochemotherapy (PUVA). Psychosomatic Medicine, 60, 625-632.
DOI: https://doi.org/10.1097/00006842-199809000-00020
Kreft, S., Kreft, M., Resman, A., Marko, P., & Kreft, K. Z. (2006). Computer-aided measurement of psoriatic lesion area in a multicenter clinical trial--comparison to physician’s estimations. Journal of Dermatological Sciences, 44, 21-27.
DOI: https://doi.org/10.1016/j.jdermsci.2006.05.006
Kross, E. K. (2015). The importance of caregivers outcomes after critical illness. Critial Care Medicine, 43 (5), 1149-1150.
DOI: https://doi.org/10.1097/CCM.0000000000000910
Lin V. W. (2012). Tough-skinned kids: identifying psychosocial effects of psoriasis and helping pediatric patients and families cope. Journal of Pediatric Nursing, 27(5), 563-572.
DOI: https://doi.org/10.1016/j.pedn.2011.10.003
Mackenzie, K. R. (1995). Effective use of group therapy in managed care. Washington, DC: American Psychiatric Press.
Manolache, L., Petrescu- Seceleanu, D. & Benea, A. (2010). Life events involvement in psoriasis onset/recurrence. International Journal of Dermatology, 49, 636-641.
DOI: https://doi.org/10.1111/j.1365-4632.2009.04367.x
Martín-Brufau, R., Romero-Brufau, S., Martín-Gorgojo, A., Brufau Redondo, C., Corbalan, J., & Ulnik, J. (2015). Psoriasis lesions are associated with specific types of emotions. Emotional profile in psoriasis. European Journal of Dermatology, 25, 329-34.
DOI: https://doi.org/10.1684/ejd.2015.2577
Michalek I. M., Loring, B., & John, S. M. (2017). A systematic review of worldwide epidemiology of psoriasis. Journal of the European Academy of Dermatology and Venereology, 31 (2), 205-212.
DOI: https://doi.org/10.1111/jdv.13854
Molina-Leyva, A., Caparros-delMoral, I., Ruiz-Carrascosa, J. C., Naranjo-Sintes, R., & Jimenez-Moleon, J. J. (2015). Elevated prevalence of Type D (distressed) personality in moderate to severe psoriasis is associated with mood status and quality of life impairment: a comparative pilot study. Journal of the European Academy of Dermatology and Venereology, 29, 1710-1717.
DOI: https://doi.org/10.1111/jdv.12960
Morisky, D. E., Green, L. W., & Levine, D. M. (1986). Concurrent and predictive validity of a self-reported measure of medication adherence. Medical Care, 67-74.
DOI: https://doi.org/10.1097/00005650-198601000-00007
Nestle, F. O., Kaplan, D. H., & Barker, J. (2009). Psoriasis. New England Journal of Medicine, 36, 1496-1509.
DOI: https://doi.org/10.1056/NEJMra0804595
Petraškienė, R., Valiukevičienė, S., & Macijauskienė, J. (2016). Associations of the quality of life and psychoemotional state with sociodemographic factors in patients with psoriasis. Medicina (Kaunas), 52(4), 238-243.
DOI: https://doi.org/10.1016/j.medici.2016.07.001
Remröd, C., Sjöström, K., & Svensson, Å. (2015). Subjective stress reactivity in psoriasis- a cross sectional study of associated psychological traits. Dermatology, 15(2), 6.
Richards, H. L., Chong, S. L. P., Mason, D. L., & Griffiths, C. E. (2002). The impact of psoriasis on healthy partners of patients with psoriasis. British Journal of Psoriasis, 147(62), 40 (Abstr).
Salman, A., Yucelten, A. D., Sarac, E., Saricam, M. H., & Perdahli-Fis, N. (2018). Impact of psoriasis in the quality of life of children, adolescents and their families: a cross-sectional study. Brasilian Dermatology, 93(6), 819-823.
DOI: https://doi.org/10.1590/abd1806-4841.20186981
Sampogna, F., Tabolli, S., Di Pietro, C., Castiglia, D., Zambruno, G., Abeni, D. (2013). The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the italian version of the family dermatology life quality index. Journal of the European Academy of Dermatology and Venerology, 27(9), 1, 151-155.
DOI: https://doi.org/10.1111/j.1468-3083.2012.04682.x
Schwartz, J., Evers, A. W. M., Bundy, C., Kimball, A. B. (2016). Getting under the skin: report from the International Psoriasis Council Workshop on the role of stress in psoriasis. Frontiers in Psychology, 7, 87.
DOI: https://doi.org/10.3389/fpsyg.2016.00087
Sobell, J. M., Foley, P., Toth, D., Mrowietz, U., Girolomoni, G., Goncalves, J., Day, R. M., Chen R., & Yosipovitch, G. (2016), Effects of apremilast on pruritus and skin discomfort/pain correlate with improvements in quality of life in patients with moderate to severe plaque psoriasis. Acta Dermato-Venereologica, 96(4), 514-520.
DOI: https://doi.org/10.2340/00015555-2360
Tadros, A., Vergou, T., Stratigos, A. J., Tzavara, C., Hletsos, M., Katsambas, A., & Antoniou, C. (2011). Psoriasis: is it the tip of the iceberg for the quality of life of patients and their families?. Journal of the European Academy of Dermatology and Venereology, 25 (11), 1282-1287.
DOI: https://doi.org/10.1111/j.1468-3083.2010.03965.x
Yalom, I., & Leszcz, M. (2005). The Theory and Practice of Group Psychotherapy (5th ed.). New York, NY: Basic Books.
Zeng, J., Luo, S., Huang, Y., & Lu Q. (2017). Critical role of environmental factors in the pathogenesis of psoriasis. Journal of Dermatology, 44(8), 863-872.
DOI: https://doi.org/10.1111/1346-8138.13806
Zigmond, A. S., & Snaith, R. P. (1983). The hospital anxiety and depression scale. Acta Psychiatrica Scandinavica, 67(6), 361-370.
DOI: https://doi.org/10.1111/j.1600-0447.1983.tb09716.x
How to Cite
Demma, A., Suitner, C. ., Ferruzza, E. ., Nicolini, C., & Donini, M. (2021). The indirect effect of a focus group for psoriatic patients on their caregivers. Research in Psychotherapy: Psychopathology, Process and Outcome, 24(1). https://doi.org/10.4081/ripppo.2021.486
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.
Similar Articles
- Emanuela Saita, Carmine Parrella, Federica Facchin, Floriana Irtelli, The Clinical Use of Photography: A Single Case, Multimethod Study of the Therapeutic Process , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 17 No. 1 (2014)
- Javier Morán, M. Francisca Díaz, Claudio Martínez, Carlos Varas, Roxana Parra Sepúlveda, The subjective experience of psychotherapists during moments of rupture in psychotherapy with adolescents , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 22 No. 1 (2019)
- Olga Fernández González, J. Carola Pérez, Mariane Krause, The relation between the therapeutic alliance and communicative intentions in therapeutic interaction during the initial phase of adolescent therapy , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 22 No. 2 (2019)
- Diego Rocco, Alessandro Gennaro, Francesco De Bei, Diego Zanelli, Valeria Condino, Development and Characteristics of the Therapeutic Alliance in a Short-Term Dynamic Psychotherapy: A Descriptive Case Study , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 16 No. 1 (2013)
- Alessia Renzi, Rachele Mariani, Michela Di Trani, Renata Tambelli, Giving words to emotions: the use of linguistic analysis to explore the role of alexithymia in an expressive writing intervention , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 23 No. 2 (2020)
- Laura Antonia Lucia Parolin, Ilaria Maria Antonietta Benzi, Erika Fanti, Alberto Milesi, Pietro Cipresso, Emanuele Preti, Italia Ti Ascolto [Italy, I am listening]: an app-based group psychological intervention during the COVID-19 pandemic , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 24 No. 1 (2021)
- Alessandra De Coro, Silvia Andreassi, Rachele Mariani, Elisabetta Iberni, Valeria Crisafulli, Adriana Matarrese, The evaluation of outcomes and process in psychotherapies offered by Mental Health Centers and an University Clinical Psychology Center , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 13 No. 2 (2010)
- Diego Rocco, Vincenzo Calvo, Vito Agrosì, Francesca Bergami, Luce Maria Busetto, Silvia Marin, Giovanna Pezzetta, Luca Rossi, Lorenzo Zuccotti, Allan Abbass, Intensive short-term dynamic psychotherapy provided by novice psychotherapists: effects on symptomatology and psychological structure in patients with anxiety disorders , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 24 No. 1 (2021)
- The Editors, Clinical practice and research: the therapeutic rhythm , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 25 No. s1 (2022): Abstract Book - XIV National Conference of the Society for Psychotherapy Research - Italian Group, Clinical practice and research: the therapeutic rhythm, November 25-26, 2022, Cremona (Italy)
- Joào F. Barreto, Paula Mena Matos, Balancing clinical risk with countertransference management protects alliance , Research in Psychotherapy: Psychopathology, Process and Outcome: Vol. 20 No. 3 (2017)
<< < 17 18 19 20 21 22 23 24 > >>
You may also start an advanced similarity search for this article.
