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1.
Pediatr Diabetes ; 22(6): 924-932, 2021 09.
Article in English | MEDLINE | ID: mdl-34173308

ABSTRACT

OBJECTIVE: Among adolescents with type 1 diabetes, research has found that their perception of their diabetes management is an important predictor of actual diabetes management. There is a need for measures that assess adolescents' perception of their ability to independently complete daily diabetes self-care tasks. The current study examined the psychometric properties of the Diabetes Skills Checklist Teen-Report (DSC-T) and DSC Parent of Teen-Report (DSC-PT), which assess perceived independence in diabetes self-care skills. RESEARCH DESIGN AND METHODS: Data were from 1450 adolescents aged 12 to 18 years and their parents who participated in the Diabetes Camp Matters Study. Families completed the DSC as well as other questionnaires online assessing demographic and diabetes-related information, diabetes strengths, and diabetes-specific emotional distress. RESULTS: Exploratory factor analysis revealed a 14-item DSC-T and 12-item DSC-PT, both with excellent internal consistency and concurrent validity. Both the DSC-T and DSC-PT were found to be positively correlated with diabetes strengths and negatively correlated with HbA1c, and the DSC-PT was significantly correlated with parent-reported diabetes distress. Adolescents who used insulin pumps and continuous glucose monitoring reported higher perceived independence in diabetes self-care skills compared to adolescents who used insulin pens/syringes or blood glucose meters. No differences were found based on demographic characteristics. CONCLUSIONS: The DSC-T and DSC-PT have strong potential to be used during diabetes clinic visits to spark discussion regarding adolescents' self-care, which would allow for a more successful transfer of diabetes care from parent to adolescent, and eventually, the transition from pediatric to adult healthcare.


Subject(s)
Diabetes Mellitus, Type 1/psychology , Self Care/psychology , Self Efficacy , Adolescent , Female , Humans , Male , Parents/psychology , Psychometrics , Reproducibility of Results
2.
Rehabil Psychol ; 66(3): 286-299, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34043409

ABSTRACT

Objective: Past research suggests that certain sociodemographic factors may put youth with spina bifida (SB) at risk for poor outcomes. The aims of this study were to examine (a) associations between ten sociodemographic factors and health-related, neuropsychological, and psychosocial functioning among youth with SB,(b) cumulative sociodemographic risk as a predictor of youth outcomes as moderated by age, and (c) SB-related family stress as a mediator of longitudinal associations between cumulative sociodemographic risk and youth outcomes. Method: Participants were youth with SB (N = 140 at Time 1; Mage at Time 1 = 11.43, 53.6% female) recruited as part of a larger, longitudinal study. The study included questionnaire (parent-, teacher-, and youth-report), neuropsychological testing, and medical chart data across three time points, spaced 2 years apart. Results: A subset of the sociodemographic factors and their cumulative risk were associated with study outcomes. Specifically, youth characterized by sociodemographic risk had greater pain and lower academic achievement, but also fewer urinary tract infections and fewer attention and executive function problems. Age did not moderate the association between cumulative risk and outcomes. Cumulative risk predicted lower SB-related family stress, which, in turn, predicted several outcomes. Conclusions: Examining a range of sociodemographic factors is warranted. Sociodemographic risk is linked to poorer outcomes for some risk indicators but similar or better outcomes for others. Results have implications for delivering evidence-based, diversity-sensitive clinical care to youth with SB. (PsycInfo Database Record (c) 2021 APA, all rights reserved).


Subject(s)
Psychosocial Functioning , Spinal Dysraphism , Adolescent , Anxiety , Female , Humans , Longitudinal Studies , Male , Parents , Spinal Dysraphism/complications
3.
Endocrinol Metab Clin North Am ; 49(1): 127-141, 2020 03.
Article in English | MEDLINE | ID: mdl-31980113

ABSTRACT

This article offers a systematic review of the literature on psychosocial aspects of technology use in children and adolescents with type 1 diabetes and their families, searching for relevant articles published the past 5 years. Topics included continuous subcutaneous insulin infusion, continuous glucose monitoring, predictive low-glucose suspend, and artificial pancreas systems. The review indicates there are positive and negative psychosocial aspects to diabetes technology use among youth and their families. Although consistent findings were revealed, contradictions exist. Discussed are recommendations for future research and implications for how health care providers can collaborate with families to discuss and manage diabetes technology.


Subject(s)
Diabetes Mellitus, Type 1/psychology , Diabetes Mellitus, Type 1/therapy , Equipment and Supplies , Perception , Adolescent , Blood Glucose Self-Monitoring/instrumentation , Blood Glucose Self-Monitoring/psychology , Child , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/drug therapy , Family/psychology , Glycemic Control/instrumentation , Glycemic Control/psychology , Humans , Insulin Infusion Systems/psychology , Inventions , Pancreas, Artificial/psychology , Parent-Child Relations
4.
J Pediatr Psychol ; 43(2): 105-119, 2018 03 01.
Article in English | MEDLINE | ID: mdl-29049792

ABSTRACT

Objective: This study examined differences in psychosocial and family functioning between Latino and non-Latino Caucasian youth with spina bifida (SB), and examined family functioning as a predictor of youth psychosocial functioning as moderated by ethnicity. Methods: Participants were part of a larger, longitudinal study (Devine, Holbein, Psihogios, Amaro, & Holmbeck, 2012) and included 74 non-Latino Caucasian youth with SB and 39 Latino youth with SB (M age = 11.53, 52.2% female). Data were collected at Time 1 and 2 years later, and included questionnaire and observational data of psychosocial and family functioning. Results: Latino youth demonstrated fewer externalizing symptoms, less family conflict, but also less social competence. Family conflict was associated with psychosocial functioning in Latino youth, while family cohesion, conflict, and stress were associated with psychosocial functioning in non-Latino Caucasian youth. Conclusions: Psychosocial and family functioning, and their relationship over time, may be different in Latino versus Caucasian youth with SB.


Subject(s)
Behavioral Symptoms/psychology , Family Relations/psychology , Hispanic or Latino/psychology , Social Skills , Spinal Dysraphism/psychology , White People/psychology , Adolescent , Child , Family Conflict/psychology , Female , Humans , Longitudinal Studies , Male
5.
J Res Adolesc ; 27(3): 566-580, 2017 09.
Article in English | MEDLINE | ID: mdl-28776835

ABSTRACT

The current study examines whether daily coping moderates the effects of daily stress on same-day mood and next-day mood among 58 Latino adolescents (Mage  = 13.31; 53% male). The daily diary design capitalized on repeated measurements, boosting power to detect effects and allowing for a robust understanding of the day-to-day experiences of Latino adolescents. Hierarchical linear modeling revealed that on days when youth reported higher levels of peer and academic stress, they also reported more negative moods. However, only poverty-related stress predicted mood the following day. Engagement coping buffered the effect of poverty-related stress on next-day negative and positive mood, while disengagement exacerbated the effects of academic and peer stress. The need for interventions promoting balanced coping repertoires is discussed.


Subject(s)
Adaptation, Psychological , Affect , Hispanic or Latino/psychology , Stress, Psychological/psychology , Adolescent , Female , Humans , Male , Narration , Poverty/psychology , Stress, Psychological/epidemiology
6.
Top Spinal Cord Inj Rehabil ; 23(1): 42-48, 2017.
Article in English | MEDLINE | ID: mdl-29339876

ABSTRACT

Sexual development and sexuality in youth with pediatric spinal cord injury (SCI) are critical areas clinicians must be aware of and discuss when working with youth and their families. In addition to the general sexuality issues and challenges of adolescence and adult development, youth with SCI face unique physical and psychosocial issues. The goal of this article is to provide a developmentally based discussion of sexuality in individuals with SCI from infancy through emerging adulthood. An overview of psychosocial issues related to sexual development and sexuality are presented for each stage of sexual development along with recommendations for clinical practice, including patient and caregiver education and counseling. In order to establish expectations for youth with SCI, long-term outcomes related to sexuality and fertility of adults with pediatric-onset SCI are presented.


Subject(s)
Sexual Behavior/psychology , Sexual Dysfunction, Physiological/etiology , Sexuality/psychology , Spinal Cord Injuries/complications , Adolescent , Adolescent Development , Child , Female , Humans , Sexual Dysfunction, Physiological/psychology , Spinal Cord Injuries/psychology
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