家庭社会经济地位与青少年自我效能感的关系：家庭支持的中介作用与性别因素的调节作用

为探讨家庭社会经济地位对青少年自我效能感的影响及其作用机制,该研究采用问卷法对520名青少年进行调查。结果表明：(1)家庭社会经济地位、家庭支持、自我效能感两两均显著正相关;女生的家庭支持显著高于男生,自我效能感显著低于男生;(2)家庭支持在家庭社会经济地位对自我效能感的影响中起中介作用;(3)该中介作用受到性别因素的调节,较之男生,女生的家庭支持受到家庭社会经济地位的影响作用更为显著。     

朋友支持与大学生幸福感：自我效能感的中介与社会比较倾向的调节

为探讨朋友支持与幸福感的关系,并重点关注自我效能感和社会比较倾向在其中所起的作用,该研究采用总体幸福感量表、一般自我效能感量表、社会比较观念量表和朋友支持评价量表对776位大学生进行施测。结果表明：（1）朋友支持正向预测大学生幸福感;自我效能感在两者间起中介作用;（2）社会比较倾向调节了社会支持→自我效能感→幸福感的后半段,即相对于高社会比较倾向的大学生而言,自我效能感对低社会比较倾向大学生的幸福感促进作用更强。该结果揭示了朋友支持影响大学生幸福感的内在机制：朋友支持和大学生幸福感之间是有调节的中介关系,朋友支持通过自我效能感影响幸福感,社会支持对间接效应起调节作用。     

农村幼儿教师的组织公平感与其职业倦怠的关系：心理授权的中介作用与家庭支持的调节作用

为探讨组织公平感对职业倦怠的影响及其作用机制,本研究使用问卷对450名农村幼儿教师进行调查。结果显示:(1)心理授权部分中介了组织公平感与职业倦怠之间的关系;(2)家庭支持调节了这一中介过程的后半路径。研究结果揭示了组织公平感对职业倦怠的影响与作用机制,对降低农村幼儿教师的职业倦怠具有重要参考价值。     

老年人微信使用与获得感的关系:领悟社会支持和生命意义感的链式中介作用

微信的普及和使用给老年人的生活带来了挑战与改变。本研究探讨了老年人微信使用强度与获得感的关系及作用机制。研究招募了916名55岁以上的老年人,采用微信使用强度量表、领悟社会支持量表、生命意义感量表和获得感量表进行施测。结果显示：(1)微信使用强度正向预测老年人的获得感;(2)领悟社会支持和生命意义感在微信使用强度和获得感之间起到单独的中介作用以及链式中介作用。研究表明,老年人的微信使用可以提升其领悟社会支持和生命意义感,从而增强他们的获得感,实现社会发展成果的共享。     

隔代照料与中老年人心理健康：家庭亲密度的中介作用

研究旨在考察隔代照料与中老年人心理健康的关系以及家庭亲密度的中介作用。采用流行病调查中心抑郁量表（CES-D）、生活满意度量表（SWLS）和家庭环境量表（FES-CV）亲密度分量表测量中老年人抑郁症状、生活满意度和家庭亲密度。自编隔代照料问卷测量中老年人的隔代照料频率。共计325位45岁及以上有照顾孙辈经验的社区中老年人参加了问卷调查。结果发现：第一,隔代照料强度与中老年人的抑郁症状、生活满意度存在显著负相关;第二,家庭亲密度部分中介了隔代照料与抑郁症状、生活满意度的负向关系。结果表明,隔代照料对中老年人心理健康既有积极作用,也有消极作用,家庭亲密度在一定程度上部分中介了上述关系。     

青少年家庭功能与亲社会行为的关系:一个有调节的中介模型

本研究采用问卷法,以1060名五至八年级学生为被试,考察了家庭功能如何通过同伴接纳的中介作用影响亲社会行为,同时探讨了留守状况在该中介模型中所起的调节作用。结果发现:(1)青少年的家庭功能、同伴接纳和亲社会行为两两之间呈显著正相关;(2)青少年的同伴接纳在家庭功能及亲社会行为中起部分中介作用;(3)留守状况调节了家庭功能通过同伴接纳影响亲社会行为的后半段路径。具体而言,与曾/现留守青少年相比,非留守青少年的家庭功能通过同伴接纳对亲社会行为产生的影响更强。研究结果可以为培养青少年的亲社会行为提供参考价值。     

权力感与助人行为：社会距离的中介和责任感的调节

本研究通过两个子研究考察权力感对助人行为的影响,及社会距离的中介作用与责任感的调节作用。研究1通过问卷法考察权力感与助人行为意愿的关系,并检验社会距离的中介作用;研究2通过实验法检验权力感对助人行为的影响,社会距离的中介作用及责任感的调节作用。结果发现,权力感以社会距离为中介,抑制助人行为;责任感能调节权力感的直接效应,控制条件下权力感抑制助人行为,责任增强条件下权力感的影响不显著。     

社会支持与大学生抑郁的关系:一个有调节的中介模型

为考察社会支持、社交焦虑、一般自我效能感和抑郁之间的关系,采用社会支持评定量表、社交焦虑量表、一般自我效能感量表以及抑郁自评量表对640名大学生进行调查。研究显示:(1)社交焦虑在社会支持与大学生抑郁之间起部分中介作用;(2)一般自我效能感在社会支持—社交焦虑—抑郁这一中介过程中的后半路径起调节作用。     

组织支持感对工作投入与工作家庭冲突关系的调节作用

在国内外研究的基础上,以207名企业员工为被试,运用问卷调查法和分层回归分析统计方法,考察了工作投入与工作家庭冲突的关系,并考察了组织支持感在工作投入与工作家庭冲突之间的调节作用。结果表明：工作投入对时间冲突和行为冲突都具有显著的负向预测作用。组织支持感在工作投入与行为冲突的关系中起调节作用。     

恶性血液病患者的社会支持、自我效能感与抑郁的关系

研究以284名恶性血液病患者为被试,采用问卷法,探讨了恶性血液病患者的社会支持、 自我效能感及抑郁水平之间的关系.结果发现:(1)恶性血液病患者抑郁得分显著高于全国常模;(2)患者自我效能感和社会支持得分呈正相关,自我效能感和社会支持与抑郁得分均呈负相关;(3)患者自我效能感在社会支持和抑郁情绪之间起部分中介作用.该结...     

Informal Caregiving to Persons with AIDS in the United States: Caregiver Burden Among Central Cities Residents Eighteen to Forty-Nine Years Old

Characteristics and caregiving experiences of friends and family members caring for people with AIDS (PWAs) were examined. Based on a probability sample of informal AIDS caregivers ages 18–49 living in central cities of the United States (n = 260), analyses were conducted to (a) identify the sociodemographic characteristics of young central city caregivers; and (b) examine the effects of caregiver characteristics (relationship to PWA, gender, race/ethnicity, income, sexual orientation, HIV status, perceived susceptibility), and level of objective caregiving demands, on subjective caregiver burden. Results indicate that the largest group of caregivers in this age category are male friends of the PWA—a group not typically found among caregivers to persons with other types of illnesses. In general, gay or bisexual caregivers, caregivers who have traditional family ties to the PWA, men relative to women, and lower income caregivers, report the greatest burden. While level of caregiving demands represents the most influential predictor of caregiver burden, white and male caregivers experience greater burden, independent of level of involvement and other caregiver characteristics. Receiving instrumental support with caregiving buffers the impact of high objective demands on subjective burden.     

Mentally retarded persons as parents: Prevalence and the situation of their children

This paper describes a research program on mentally retarded parents and their children. For this nation-wide study, two structured questionnaires were sent to all municipalities in Norway. Both questionnaires were sent to public health nurses and were followed-up by a structured telephone interview based on the questionnaires. The primary aim of the study was to survey the number of children born to mentally retarded parents. In addition, the children's needs and functional abilities were to be assessed. Twenty-three mentally retarded persons had given birth in the course of the past twelve months. A total of 126 children with mentally retarded parents were identified, with an incidence of 27 children per year, and a prevalence of approximately 430 children under 16 years of age in a population of 4 mill. People with a mean of 1.05 child per family. About 43% of the children of mentally retarded parents appeared to have learning difficulties. Forty percent of the children suffered from failures of care. Between 25% and 68% of the children with learning problems had poorly developed motor or language abilities, sense modalities or psycho-social status.     

Preparing Students for Family Practice

This paper highlights the content of a course designed to prepare students for family practice, with emphasis on mothers as primary caregivers. A model is presented of relatively healthy family interactions characterized by co-parenting and equitable division of labor in the home. The strengths perspective is applied to family practice with mother-headed families where noncustodial fathers share responsibilities for childrearing. Challenges inherent in carrying out dual roles of wage labor and family caregiving are linked to social support and differences among women based on class, race, and ethnicity.     

Another Side to Caregiving: Negative Reactions to Being Helped

Until recently, caregiving research focused almost exclusively on caregivers of older adults with health problems, and there was little focus on care recipients' perceptions of the care they receive. The present article reviews relevant research on reactions to caregiving assistance. Several recent studies indicate that help in these contexts can be viewed negatively by care recipients. As many as two thirds of physically impaired older adults who receive assistance with daily activities, such as preparing meals, climbing stairs, or dressing, experience negative reactions to some of the help they receive. Negative reactions seem to have important consequences for the care recipient, because they are associated with higher depression concurrently and 1 year later. Because some of the findings are inconsistent with theoretical models of negative responses to help, an alternative framework, based on social-support and social-conflict research, is briefly proposed.     

Impact of Psychoeducational Interventions on Distressed Family Caregivers

This study compared the effectiveness of two active interventions to a waiting-list control condition to reduce depression and burden and increase use of adaptive coping strategies in family caregivers (N = 161) of physically and/or cognitively impaired older adults. Chi-square analysis of change in depression status from pre- to postintervention showed a higher percentage of improvement among participants in the increasing life satisfaction psychoeducational condition compared to the improvement rate in either the problem-solving psychoeducational class or the wait-list condition. Change in coping strategies and subjective level of burden also differed by group, with participants in the class conditions reporting more frequent use of cognitive or behavioral coping strategies, and less subjective burden, from pre- to postintervention. There was no change in either avoidant coping or perceived stress over time. Results show that intervention programs targeted to improve specific coping skills and psychological symptoms can have a significant impact on caregivers' distress.     

The Complexity of Support: The Impact of Family Structure and Provisional Support on African American and White Adolescent Mothers' Well-Being

The importance of social support to the well-being of adolescent parents is a frequently discussed topic in the teen parenting literature. However, the meaning and conceptualization of social support varies across study and the heterogeneity within the teen parent population is often overlooked. In an effort to understand its role more precisely, the present study defined support both in terms of its structural and provision components, and examined the association of these components with both perceived psychological and behavioral measures of maternal well-being for a sample of white and African American teen mothers. Specifically, the relative contribution of household structure and provisional social support to the well-being of a sample of 107 African American and 146 white teen mothers was measured respectively. Results indicate great variability in the structural and provisional support adolescent mothers receive, regardless of race. Independent of other effects, provisional supports are more strongly associated with maternal well-being than is family structure. Further, the impact of these different types of support varies by race.     

Involving Family in Psychosocial Interventions for Chronic Illness

ABSTRACT— Interactions with close family members have consequences for the emotional and physical well-being of individuals who are dealing with a chronic physical illness. Therefore, inclusion of a close family member in psychosocial interventions for chronic illnesses is a logical treatment approach that has the potential to boost the effects of intervention on the patient and also benefit the family member. However, randomized, controlled studies indicate that such family-oriented interventions generally have small effects. The efficacy of these treatment approaches might be enhanced by targeting specific interactions that emerging research identifies as promoting or derailing healthy behaviors and by better incorporating strategies from family caregiver interventions. In addition, family-oriented interventions should be more fully evaluated, by assessing the benefits for both patients and family members. Future research in this area can tell us much about how and when to involve family in treatment of specific chronic illnesses and, in turn, may inform conceptual models of the impact of family interactions on health.     

Assessment-based intervention for severe behavior problems in a natural family context.

Functional assessments and assessment-based interventions were conducted with a boy with disabilities and severe problem behavior in the context of two family routines: using the bathroom in the family home and dining in a fast-food restaurant. A multiple baseline design demonstrated the effectiveness of the intervention package as implemented by the boy's mother in the two routines. The results provide a systematic replication and extension of behavior-analytic interventions in natural family contexts.