Análise Fatorial Exploratória do Questionário de Percepção de Doenças Versão Breve (Brief IPQ)

Nogueira, Graziela Sousa; Seidl, Eliane Maria Fleury; Tróccoli, Bartholomeu Tôrres

doi:10.1590/0102-37722016011871161168

Cited by 10 publications

(11 citation statements)

References 19 publications

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“…O escore médio igual a 70,40 no CD-RISC revelou que os participantes estavam com bons níveis de resiliência, mas com variabilidade na amostra. Quanto à percepção de doença, os resultados também foram bons, já que a média foi igual a 26,23, e quanto mais baixo o escore − em especial menor que 33, ponto de corte estabelecido no estudo de validação (Nogueira & Seidl, 2016a) −, menos evidência de que a condição é percebida como muito ameaçadora e de forma negativa. O coeficiente de correlação negativo e significativo entre essas duas variáveis fez sentido, pois escores mais altos em resiliência estiveram associados à percepção menos negativa e ameaçadora da soropositividade, indo ao encontro da literatura (Cal et al, 2015;Nogueira & Seidl, 2016a).…”

Section: Discussionunclassified

“…Estudo com pessoas brasileiras soropositivas para o HIV observou correlação positiva estatisticamente significativa entre escores mais altos em percepção de doença (indicativos de percepções ameaçadoras da enfermidade) e ocorrência de ansiedade e depressão. Os resultados mostraram ainda correlação negativa significativa entre percepção de doença e autoeficácia para adesão à TARV, permitindo concluir que quanto maior a percepção negativa e de ameaça da infecção pelo HIV, menor a autoeficácia percebida para aderir aos ARVs (Nogueira & Seidl, 2016a).…”

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Adesão ao Tratamento, Resiliência e Percepção de Doença em Pessoas com HIV,

Seidl

Remor

2020

Psic.: Teor. e Pesq.

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Resumo O objetivo deste estudo foi investigar variáveis preditoras da adesão ao tratamento antirretroviral entre aspectos sociodemográficos, clínicos e psicológicos (resiliência e percepção de doença) em pessoas com o vírus da imunodeficiência humana (HIV). Participaram 155 pacientes, sendo 72,9% homens. Roteiros de entrevista sobre aspectos sociodemográficos e clínicos e instrumentos validados para a população brasileira foram aplicados. Três variáveis foram preditoras da adesão: resiliência, percepção de doença como preditor negativo, e idade, totalizando 29% de variância explicada. O estudo tem implicações para a prática de psicólogos e de equipes de saúde que atuam na área, com base na implementação de intervenções visando à adesão e ao autocuidado, bem como à adaptação e à resiliência em pessoas que vivem com HIV.

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Adesão ao Tratamento, Resiliência e Percepção de Doença em Pessoas com HIV,

Seidl

Remor

2020

Psic.: Teor. e Pesq.

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“…1) Demographics, disease and treatment variables (age, age at diagnosis, type of cancer, treatment, and recurrence) were collected from the patient’s medical records.2) Brief Illness Perception Questionnaire (Brief IPQ) (Broadbent et al, 2006), Brazilian–Portuguese version (Nogueira et al, 2016): Brief-IPQ is a 9 item self-reported measure (range 0–10), a short version derived from the Revised Illness Perception Questionnaire (IPQ-R) (Moss-Morris et al, 2002). The measure has been used in a variety of chronic conditions and has been administrated to adolescents and adult patients (Broadbent et al, 2015).…”

Section: Methodsmentioning

confidence: 99%

Illness perceptions in childhood cancer survivor and caregivers’ dyads

Castro

Beltrão

Armiliato

et al. 2022

Clin Child Psychol Psychiatry

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Surviving childhood cancer is a difficult experience for children and their caregivers, it can produce long-term emotional distress. Illness perceptions refer to the way people understand the different aspects related to illness from their individual and collective experiences. Objective: to compare the illness perceptions of adolescent childhood cancer survivors and their caregivers and examine the relationship between illness perception of childhood cancer survivors, their caregivers, and sociodemographic, illness, and treatment variables. Forty-three survivor-caregiver dyads (the mean age of a survivor 17.05 years old; the mean age of caregivers 47.53 years old) participated in the study and answered the Brief Illness Perception Questionnaire (Brief IPQ) and Demographics data. Results: Results showed significant differences in the illness perceptions of survivors and caregivers. Caregivers presented more negative cognitive perceptions than survivors (t = −6.701, p < 0.001), especially in the identity dimension (t = −4.327, p < 0.001), and more negative emotional perceptions than survivors (t = −4.132, p < 0.001), both in concern (t = −3.695, p < 0.001) and emotional representation (t = −3.466, p < 0.001). No significant correlations were found between survivors' and caregivers' illness perceptions and sociodemographic illness variables. Conclusion: These findings showed that even though dyads went through cancer together, survivors’ and caregivers' perceptions of childhood cancer are different, indicating the need to better understand how children growing up with a chronic disease develop such illness perceptions and their experience.

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“…It has nine items composed of a scale ranging from zero to 10 each. The items covered are related to cognitive assessment of the disease, emotional representation, and comprehension of the disease 20 . The scores range from zero to 80 and the higher the score, the greater the perception of threat of the disease.…”

Section: Assessment Instrumentsmentioning

confidence: 99%

The positives effects of a pain education program on patients with chronic pain: observational study

Pontin¹,

Gioia²,

Dias³

et al. 2021

Brazilian Journal of Pain

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BACKGROUND AND OBJECTIVES:Pain education is a tool that helps health professionals in the biopsychosocial approach and in pain management in patients with musculoskeletal pain. The objectives of the study were to verify the effects of a pain education program in patients with chronic musculoskeletal pain. The evaluated outcomes were pain, kinesiophobia, catastrophizing, quality of life, central sensitization and perception of the disease. METHODS: Observational, retrospective study. Data from 24 participants with chronic pain, mean age 57 years, were analyzed, 83% of whom were female. Patients participated in a pain education program, which addressed topics such as acceptance, pain alarm, sleep, relaxation, negative thoughts, return to activities, relationships, and exercises. RESULTS: Participants showed significant changes in the cognitive representation of the disease measured by the Illness Perception Questionnaire (Brief-IPQ) (p<0.01), central sensitization by the CSI (p=0.05), catastrophism (p<0.05), pain (p<0.01), physical aspects by the Short-Form Health Survey (SF-36) (p<0.05) and in the total score of the same Instrument (p<0.05). CONCLUSION: The group applied pain education associated with usual physical therapy had significant effects in relation to the cognitive representation of the disease, central sensitization, catastrophizing and quality of life in patients with chronic musculoskeletal pain.

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Análise Fatorial Exploratória do Questionário de Percepção de Doenças Versão Breve (Brief IPQ)

Cited by 10 publications

References 19 publications

Adesão ao Tratamento, Resiliência e Percepção de Doença em Pessoas com HIV,

Adesão ao Tratamento, Resiliência e Percepção de Doença em Pessoas com HIV,

Illness perceptions in childhood cancer survivor and caregivers’ dyads

The positives effects of a pain education program on patients with chronic pain: observational study

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