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1.
Support Care Cancer ; 26(12): 4199-4206, 2018 Dec.
Article in English | MEDLINE | ID: mdl-29948397

ABSTRACT

PURPOSE: The goals of this study were to assess the feasibility of a web-based application-electronic Social Network Assessment Program (eSNAP)-to automate the capture and visualization of family caregiver social network data of neuro-oncology patients. METHODS: Caregivers were recruited from a neuro-oncology clinic at an NCI-designated comprehensive cancer center. Participants completed baseline questionnaires on a laptop in clinic assessing demographic characteristics. After baseline, participants were randomly assigned to either create a social network visualization using eSNAP (intervention) or to usual care (control) condition. Those who used eSNAP provided likeability/usability data. All participants were asked to complete follow-up questionnaires at 3 and 6 weeks after baseline to determine feasibility of longitudinal study. RESULTS: We recruited 40 caregivers of patients with primary malignant brain tumor to participate in this study. Participants rated eSNAP usability and likeability highly, indicating that eSNAP would help them consider their available social support. At 3 weeks, 90% of participants completed questionnaires and 82.5% completed questionnaires at 6 weeks. CONCLUSIONS: There is a need to encourage family caregivers of patients with primary malignant brain tumor to engage their existing social network resources to help alleviate caregiver burden. Our findings suggest that our web-based application to address this issue is feasible to implement with high usability and likeability. This pilot study identified minor changes to the intervention to improve effectiveness and has implications for future research in this understudied population. TRIAL REGISTRATION: clinicaltrials.gov, protocol number NCT03026699.


Subject(s)
Ambulatory Care Facilities/standards , Caregivers/psychology , Medical Oncology/methods , Neurology/methods , Social Support , Adult , Aged , Aged, 80 and over , Feasibility Studies , Female , Humans , Longitudinal Studies , Male , Middle Aged , Pilot Projects , Surveys and Questionnaires
2.
Oncol Nurs Forum ; 45(1): 69-76, 2018 01 01.
Article in English | MEDLINE | ID: mdl-29251285

ABSTRACT

OBJECTIVES: To explore the feasibility and acceptability of use of a smartphone medication reminder application to promote adherence to oral medications among adolescents and young adults (AYAs) with cancer.
. SAMPLE & SETTING: 23 AYAs with cancer from a Children's Oncology Group-affiliated children's hospital and a National Cancer Institute-designated comprehensive cancer center in Salt Lake City, UT.
. METHODS & VARIABLES: Participants were asked to use the application for eight weeks. Data on application usage were obtained from a cloud-based server hosted by the application developers. Weekly self-report questionnaires were completed. Feasibility was assessed through participants' usage and responses. Acceptability was assessed through participants' perceived ease of use and usefulness.
. RESULTS: Almost all participants used the application at least once. More than half reported that they took their medications immediately when they received reminders. Participants also reported that the application was easy to set up and use, and that it was useful for prompting medication taking.
. IMPLICATIONS FOR NURSING: Nurses could continue to test the efficacy of integrating e-health modalities, such as smartphone applications, into efforts to promote medication adherence.


Subject(s)
Antineoplastic Agents/therapeutic use , Medication Adherence/statistics & numerical data , Neoplasms/drug therapy , Reminder Systems/instrumentation , Reminder Systems/statistics & numerical data , Self Care/instrumentation , Smartphone , Adolescent , Adult , Female , Humans , Male , Self Care/methods , Surveys and Questionnaires , Telemedicine/instrumentation , Telemedicine/methods , Utah , Young Adult
3.
J Cancer Educ ; 33(1): 214-221, 2018 02.
Article in English | MEDLINE | ID: mdl-27592022

ABSTRACT

Assessments of cancer survivors' health-related needs are often limited to national estimates. State-specific information is vital to inform state comprehensive cancer control efforts developed to support patients and providers. We investigated demographics, health status/quality of life, health behaviors, and health care characteristics of long-term Utah cancer survivors compared to Utahans without a history of cancer. Utah Behavioral Risk Factor Surveillance System (BRFSS) 2009 and 2010 data were used. Individuals diagnosed with cancer within the past 5 years were excluded. Multivariable survey weighted logistic regressions and computed predictive marginals were used to estimate age-adjusted percentages and 95 % confidence intervals (CI). A total of 11,320 eligible individuals (727 cancer survivors, 10,593 controls) were included. Respondents were primarily non-Hispanic White (95.3 % of survivors, 84.1 % of controls). Survivors were older (85 % of survivors ≥40 years of age vs. 47 % of controls). Survivors reported the majority of their cancer survivorship care was managed by primary care physicians or non-cancer specialists (93.5 %, 95 % CI = 87.9-99.1). Furthermore, 71.1 % (95 % CI = 59.2-82.9) of survivors reported that they did not receive a cancer treatment summary. In multivariable estimates, fair/poor general health was more common among survivors compared to controls (17.8 %, 95 % CI = 12.5-23.1 vs. 14.2 %, 95 % CI = 12.4-16.0). Few survivors in Utah receive follow-up care from a cancer specialist. Provider educational efforts are needed to promote knowledge of cancer survivor issues. Efforts should be made to improve continuity in follow-up care that addresses the known issues of long-term survivors that preclude optimal quality of life, resulting in a patient-centered approach to survivorship.


Subject(s)
Aftercare , Health Behavior , Neoplasms/therapy , Outcome Assessment, Health Care , Quality of Life , Survivors/statistics & numerical data , Adolescent , Adult , Aged , Aged, 80 and over , Behavioral Risk Factor Surveillance System , Case-Control Studies , Child , Child, Preschool , Female , Health Status , Humans , Infant , Male , Middle Aged , Surveys and Questionnaires , Survivors/psychology , Utah , Young Adult
4.
J Pediatr Psychol ; 35(8): 837-47, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20185416

ABSTRACT

OBJECTIVES: To conduct a pilot study examining whether adding biofeedback-assisted relaxation training (BART) to medication treatment results in better clinical outcomes than medication treatment alone for children with functional dyspepsia (FD) associated with duodenal eosinophilia, a subgroup of children with recurrent abdominal pain. METHODS: Twenty children were randomly assigned to receive a standardized medication treatment or medication plus 10 sessions of BART. Children and parents completed psychosocial functioning and quality of life measures at baseline, posttreatment, and 6 months. Children rated pain daily via PDA. Physicians provided biweekly assessments of clinical improvement. RESULTS: Children receiving medication plus BART demonstrated better outcomes on pain intensity, duration of pain episodes, and clinical improvement than children receiving medication alone. CONCLUSIONS: BART is a promising adjunctive treatment for pediatric FD associated with duodenal eosinophilia. Electronic daily diaries appear to be a useful approach to assessing changes in self-reported pain ratings in this population.


Subject(s)
Biofeedback, Psychology/methods , Duodenal Diseases/therapy , Dyspepsia/therapy , Eosinophilia/therapy , Relaxation Therapy/methods , Abdominal Pain/therapy , Adolescent , Analysis of Variance , Child , Combined Modality Therapy , Duodenal Diseases/complications , Dyspepsia/complications , Eosinophilia/complications , Female , Humans , Male , Pain Measurement , Pilot Projects , Quality of Life , Surveys and Questionnaires , Treatment Outcome
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