Sense of Competence Questionnaire

Vernooij‐Dassen, Myrra; Persoon, Jean; Felling, A.J.A.

doi:10.1037/t14713-000

Cited by 4 publications

(8 citation statements)

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“…Five outcome measures were identified for the construct of self-efficacy: The Revised Scale for Caregiving Self-Efficacy (RSSE; Steffen et al , 2002), the Self-Efficacy Questionnaire for Chinese Family Caregivers (Zhang et al , 2012), Family Caregivers’ Self-Efficacy for Managing Dementia Scale (Fortinsky et al , 2002), the Sense of Competence Questionnaire (SCQ; Vernooij-Dassen, 1993; Vernooij-Dassen et al , 1996), and its short version, the Short Sense of Competence Questionnaire (SSCQ: Vernooij-Dassen et al , 1999).…”

Section: Resultsmentioning

confidence: 99%

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Positive psychology outcome measures for family caregivers of people living with dementia: a systematic review

Stansfeld

Stoner

Wenborn

et al. 2017

Int. Psychogeriatr.

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There are some robust positive measures in existence for family caregivers of people living with dementia. However, lack of reporting of the psychometric properties hindered the quality assessment of some outcome measures identified in this review. Future research should aim to include positive outcome measures in interventional research to facilitate a greater understanding of the positive aspects of caregiving and how these contribute to well-being.

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Section: Resultsmentioning

confidence: 99%

“…The SCQ (Vernooij-Dassen, 1993) scored moderately on the quality assessment criteria (6/18). The SCQ had good internal consistency overall (α = 0.79) but the subscales did not show good Cronbach's alpha scores, ranging from α = 0.5 to α = 0.63.…”

Section: Resultsmentioning

confidence: 99%

Positive psychology outcome measures for family caregivers of people living with dementia: a systematic review

Stansfeld

Stoner

Wenborn

et al. 2017

Int. Psychogeriatr.

View full text Add to dashboard Cite

show abstract

“…20,27,28 The SCQ aims to assess the informal caregiver's feelings of being capable of caring for the patient. 21 The SCQ consists of 27 items on three subscales: satisfaction with the patient as a recipient of care, satisfaction with one's own performance as a caregiver and consequences of involvement in care for the personal life of the caregiver. 2,21 The SCQ has been applied in caregivers of stroke patients before.…”

Section: Instruments For Assessing Burdenmentioning

confidence: 99%

“…In this paper we compare three often used measures of subjective burden of informal caregiving in a population of informal caregivers for stroke patients, i.e., the Caregiver Strain Index (CSI), 13 Caregiver Reaction Assessment (CRA), 20 and Sense of Competence Questionnaire (SCQ). 21 In addition, we compare these measures with a self-developed single question on self-rated burden (SRB). Our purpose is to evaluate whether the simpler and more concise CSI and one-item SRB perform as well as the CRA and the SCQ in terms of feasibility, convergent validity and clinical validity.…”

Section: Introductionmentioning

confidence: 99%

Instruments for assessing the burden of informal caregiving for stroke patients in clinical practice: a comparison of CSI, CRA, SCQ and self-rated burden

et al. 2004

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A concise and simple measure would facilitate early detection of caregivers at risk in clinical practice and research. CSI and SRB are more feasible and at least as valid instruments for assessment of caregiver burden in stroke than the longer and more complex SCQ and CRA. SRB could be used for quick screening of caregivers at risk. CSI is indicated for further diagnosis of the burden of informal caregivers.

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“…The information of both the NPI and DAD is obtained from a caregiver familiar with the patient’s behaviour by means of a semi structured interview. Caregiver’s burden of care is assessed using the disease specific Sense of Competence Questionnaire (SoCQ) [ 20 , 21 ].…”

Section: Methodsmentioning

confidence: 99%

Diagnostic and economic evaluation of new biomarkers for Alzheimer’s disease: the research protocol of a prospective cohort study

et al. 2012

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BackgroundNew research criteria for the diagnosis of Alzheimer’s disease (AD) have recently been developed to enable an early diagnosis of AD pathophysiology by relying on emerging biomarkers. To enable efficient allocation of health care resources, evidence is needed to support decision makers on the adoption of emerging biomarkers in clinical practice. The research goals are to 1) assess the diagnostic test accuracy of current clinical diagnostic work-up and emerging biomarkers in MRI, PET and CSF, 2) perform a cost-consequence analysis and 3) assess long-term cost-effectiveness by an economic model.Methods/designIn a cohort design 241 consecutive patients suspected of having a primary neurodegenerative disease are approached in four academic memory clinics and followed for two years. Clinical data and data on quality of life, costs and emerging biomarkers are gathered.Diagnostic test accuracy is determined by relating the clinical practice and new research criteria diagnoses to a reference diagnosis. The clinical practice diagnosis at baseline is reflected by a consensus procedure among experts using clinical information only (no biomarkers). The diagnosis based on the new research criteria is reflected by decision rules that combine clinical and biomarker information. The reference diagnosis is determined by a consensus procedure among experts based on clinical information on the course of symptoms over a two-year time period.A decision analytic model is built combining available evidence from different resources among which (accuracy) results from the study, literature and expert opinion to assess long-term cost-effectiveness of the emerging biomarkers.DiscussionSeveral other multi-centre trials study the relative value of new biomarkers for early evaluation of AD and related disorders. The uniqueness of this study is the assessment of resource utilization and quality of life to enable an economic evaluation. The study results are generalizable to a population of patients who are referred to a memory clinic due to their memory problems.Trial registrationNCT01450891

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Sense of Competence Questionnaire

Cited by 4 publications

References 0 publications

Positive psychology outcome measures for family caregivers of people living with dementia: a systematic review

Positive psychology outcome measures for family caregivers of people living with dementia: a systematic review

Instruments for assessing the burden of informal caregiving for stroke patients in clinical practice: a comparison of CSI, CRA, SCQ and self-rated burden

Diagnostic and economic evaluation of new biomarkers for Alzheimer’s disease: the research protocol of a prospective cohort study

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