Help-seeking: An understudied problem-solving skill in children

Traditional approaches to the study of young children's behavior in helping relationships are examined and criticized as inadequate because they have failed to represent the child's perspective from the role of “active helpee” (i.e., help-seeker in such relationships). By failing to look at helping from the perspective of the one who seeks help, researchers have neglected to pursue an important lead in understanding why some children are able to learn and progress independently when confronted with the same obstacles that serve to defeat other children. This article focuses on instrumental help-seeking defined as an active, complex social-cognitive activity that is essential to learning and achievement. In the first sections of this article, it is argued that instrumental help-seeking can be formally distinguished from passive dependency as well as from the actual giving and receiving of help. In following sections, a heuristic model of the help-seeking process is offered, prior research relevant to the model is reviewed, and ideas for research on help-seeking in children are suggested within the framework of this model.     

Caregivers’ beliefs about dementia: findings from the IDEAL study

Abstract

Objective: Informal caregivers of people with dementia develop their own beliefs about the condition, referred to as Dementia Representations (DRs), as they try to make sense of the changes they are observing. The first aim of this study was to provide a profile of the types of DRs held by caregivers. The second aim was to examine the impact of caregivers’ DRs on their well-being, satisfaction with life (SwL) and caregiving stress.

Methods: Participants were 1264 informal caregivers of people in the mild-to-moderate stages of dementia from time-point 1 of the IDEAL cohort study.

Measures: DRs were measured using questionnaire items covering: Identity, Cause, Control, and Timeline.

Results: Almost half (49.2%) of caregivers used a diagnostic term to describe the person’s condition, although 93.4% of caregivers stated they were aware of the diagnosis. Higher well-being, SwL, and lower caregiving stress were associated with the use of an identity term relating to specific symptoms of dementia, attributing the cause to ageing or not knowing the cause, and believing the condition would stay the same. Lower well-being, SwL, and higher caregiving stress were associated with believing there was little that could be done to control the effects of the condition.

Conclusion: Healthcare professionals should assess and gain an understanding of caregivers’ DRs in order to provide more tailored information and support.