Research has shown that a significant proportion of advanced cancer patients'family caregivers (30% to 50%) experience clinically significant distress. Lung cancer is the most common cause of cancer deaths, and patients with this disease experience more symptom distress relative to patients with other cancer types, which may increase care-giving demands. Currently, there is limited knowledge of the reasons that cancer patients'family caregivers underutilize psychosocial support services, and there is a paucity of research-based interventions that are tailored to the needs of this population. In this study, a sample of primary family caregivers (e.g., spouses, adult children;N = 80) with clinically significant distress will be recruited to complete individual phone assessments approximately 4 to 6 weeks after the patient's lung cancer diagnosis and three months later. A subsample (n = 30) that has not accessed psychosocial services over the study period will also complete a qualitative interview within 2 weeks of the 3- month follow-up. The study aims are to examine: (1) psychosocial and practical needs of primary family caregivers of lung cancer patients;(2) psychosocial and practical barriers to psychosocial support service use in this population;and (3) family caregivers'preferences (preferred topics, modality, provider, timing) regarding psychosocial support interventions. Finally, the extent to which theory-driven demographic and psychosocial variables at baseline predict subsequent psychosocial support service use among family caregivers will be assessed. Results will directly inform the design and delivery of new psychosocial interventions that are tailored to the needs of lung cancer patients'family caregivers. In addition, this study will provide new and valuable information for identifying distressed family caregivers of lung cancer patients who are less likely to use psychosocial support services and developing strategies to increase appropriate use of these services.

Public Health Relevance

Over 500,000 cancer deaths occur each year, and lung cancer is the most common cause of these deaths. Although family caregivers of cancer patients exhibit a need for psychosocial services, these services are underutilized, and few research-based psychosocial interventions have been developed for this population. The proposed longitudinal study examines psychosocial and practical needs, barriers to psychosocial service use, and psychosocial service preferences of lung cancer patients'family caregivers, which will directly inform future intervention trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
7R03CA139862-02
Application #
7880250
Study Section
Special Emphasis Panel (ZCA1-SRLB-H (J1))
Program Officer
O'Mara, Ann M
Project Start
2009-09-01
Project End
2012-08-31
Budget Start
2010-09-01
Budget End
2012-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$77,000
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Mosher, C E; Given, B A; Ostroff, J S (2015) Barriers to mental health service use among distressed family caregivers of lung cancer patients. Eur J Cancer Care (Engl) 24:50-9
Mosher, Catherine E; Jaynes, Heather A; Hanna, Nasser et al. (2013) Distressed family caregivers of lung cancer patients: an examination of psychosocial and practical challenges. Support Care Cancer 21:431-7
Mosher, Catherine E; Champion, Victoria L; Azzoli, Christopher G et al. (2013) Economic and social changes among distressed family caregivers of lung cancer patients. Support Care Cancer 21:819-26
Mosher, Catherine E; Champion, Victoria L; Hanna, Nasser et al. (2013) Support service use and interest in support services among distressed family caregivers of lung cancer patients. Psychooncology 22:1549-56