Predictors of caregiver depression among community-residing families living with traumatic brain injury

NeuroRehabilitation

Volumn 22, Issue 1, 2007, Pages 3-8

  Rivera, Patricia ^a   Elliott, Timothy R ^b   Berry, Jack W ^a   Grant, Joan S ^a   Oswald, Kimberly ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b TEXAS A AND M UNIVERSITY   (United States)

Author keywords

Caregivers; Depression; Traumatic brain injury

Indexed keywords

ADULT; AGED; ARTICLE; CAREGIVER; CAREGIVER BURDEN; CENTER FOR EPIDEMIOLOGICAL STUDIES DEPRESSION SCALE; CORRELATION ANALYSIS; DEMOGRAPHY; DEPRESSION; FEMALE; HUMAN; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MALE; PROBLEM SOLVING; TRAUMATIC BRAIN INJURY;

EID: 33947411860     PISSN: 10538135     EISSN: None     Source Type: Journal    
DOI: 10.3233/nre-2007-22102     Document Type: Article

References (36)

1. J.K. Harris, H.P.D. Godfrey, F.M. Partridge and R.G. Knight, Caregiver depression following traumatic brain injury (TBI): a consequence of adverse effects on family members? Brain Injury, 15 (2001), 223-238.
2. R. Wells, J. Dywan and J. Dumas, Life satisfaction in family caregivers as related to specific behavioral changes after traumatic brain injury, Brain Injury 19 2005, 1105-1115.
3. A. Perlesz, G. Kinsella and S. Crowe, Impact of traumatic brain injury on the family: A critical review, Rehabilitation Psychology 44 (1999), 6-35.
4. A. Nezu, Problem solving and behavior therapy revisited. Behavior Therapy, 35 (2004), 1-33.
5. J. Kreutzer, J. Marwitz and K. Kepler, Traumatic brain injury: Family response and outcome. Archives of Physical Medicine and Rehabilitation 73 (1993), 771-778.
6. J.M. Douglas and F.J. Spellacy, Correlates of depression in adults with severe traumatic brain injury and their carers, Brain Injury 14 (2000), 71-88.
7. C. Boake, Supervision Rating Scale: A measure of functional outcome from brain Injury, Archives of Physical Medicine Rehabilitation 77 (1996), 765-772.
8. J. Rivara, K. Jaffe, N. Polissar, L.S. Fay and K. Martin, Predictors of family functioning and change 3 years after traumatic brain injury in children, Archives of Physical Medicine Rehabilitation 77 (1996), 754-764.
9. M.G. Livingstone, Effects on the family system, in: Rehabilitation of the Adult and Child with Traumatic Brain Injury, M. Rosenthal, E.R. Griffith, M.R. Bond and J.D. Miller, eds, 2nd ed., Philadelphia: Davis, 1990, pp. 225-233.
10. T. Ergh, L. Rapport, R. Coleman and R. Hanks, Predictors of caregiver and family functioning following traumatic brain injury: social support moderates caregiver distress.
11. G.P. Prigatano, S. Borgaro, J. Baker and J. Wethe, Awareness and Distress After Traumatic Brain Injury: A Relative's Perspective, J Head Trauma Rehabilitation 20(4) (2005), 359-367,
12. Journal of Head Trauma Rehabilitation 17 (2002), 155-174.
13. K. Chwalisz, The perceived stress model of caregiver burden: Evidence from the spouses of persons with brain injuries, Rehabilitation Psychology 41 (1996), 91-114.
14. W.E. Haley, D. Waff, M. Coleton, G. Ford, C. West, R. Collins and T. Isobe, Appraisal, coping, and social support as mediators of well-being in Black and White family caregivers of patients with Alzheimer's disease, Journal of Consulting and Clinical Psychology 64 (1996), 121-129.
15. K. Hooker, D. Monahan, K. Shifren and C. Hutchinson, Mental and physical health of spouse caregivers: The role of personality, Psychology and Aging 7 (1992), 367-375.
16. T. Elliott and M. Kurylo, Hope over disability: Lessons from one young woman's triumph, in: The Handbook of Hope: Theory, Measures, and Applications, C.R. Snyder, ed., New York: Academic Press, 2000, pp. 373-386.
17. A. Nezu and M.G. Perri, Social problem solving therapy for unipolar depression: An initial dismantling investigation, Journal of Consulting and Clinical Psychology 57 (1989), 408-413.
18. G. Kinsella, B. Ong, D. Murtagh, M. Prior and M. Sawyer, The role of the family for behavioral outcome in children and adolescents following traumatic brain injury, Journal of Consulting and Clinical Psychology 67 (1999), 116-123.
19. M. Pinquart, and S. Sorensen, Differences between caregivers and non-caregivers in psychological health and physical health: A meta-analysis, Psychology and Aging, 18 (2003), 250-267.
20. L.R. Leach, R.G. Frank, D.E. Bouman and J. Farmer, Family functioning, social support and depression after traumatic brain injury, Brain Injury 8 (1994), 599-606.
21. T. Elliott, J.S Grant and D. Miller, Social problem solving abilities and behavioral health, in: Social Problem Solving: Theory, Research, and Training, E. Chang, T.J. D'Zurilla and L.J. Sanna, eds, Washington, D.C., American Psychological Association, 2004, pp. 117-133.
22. J. Grant, M. Weaver, T. Elliott, A. Bartolucci and J. Newman-Giger, Family caregivers of stroke survivors: Characteristics of caregivers at risk for depression, Rehabilitation Psychology 49 (2004), 172-179.
23. J.S. Grant, T. Elliott, M. Weaver, A. Bartolucci and J. Giger, A telephone intervention with family caregivers of stroke survivors after rehabilitation, Stroke 33 (2002), 2060-2065.
24. T.R. Elliott, R. Shewchuk and J. Richards, Family caregiver social problem-solving abilities and adjustment during the initial year of the caregiving role, Journal of Counseling Psychology 48 (2001), 223-232.
25. T.R. Elliott, R. Shewchuk, J.S. Richards, Caregiver social problem-solving abilities and family member adjustment to recent-onset physical disability, Rehabilitation Psychology 44 (1999), 104-123.
26. P.P. Vitaliano, J. Zhang and J. Scanlan, Is caregiving hazardous to one's physical health? A meta-analysis, Psychological Bulleting 129 (2003), 946-972.
27. R. Schulz and S. Beach, Caregiving as a risk factor for mortality: The caregiver health effects study, Journal of the American Medical Association 282 (1999), 2215-2219.
28. R. Shewchuk, J. Richards and T. Elliott, Dynamic processes in the first year of a caregiving career, Health Psychology 17 (1998), 125-129.
29. M.F. Folstein, S.E. Folstein and P.R. McHugh, Mini-Mental State: A practical method for grading the state of patients for the clinician, Journal of Psychiatric Research 12 (1975), 189-198.
30. T. D'Zurilla, A. Nezu and A. Maydeu-Olivares, Social Problem-Solving Inventory-Revised (SPSI-R): Manual, North Tonawanda, NY, Multi-Health Systems, 2002.
31. P. Carey, M.T. Oberst, M.A. McCubbin et al., Appraisal and caregiving burden in family members caring for patients receiving chemotherapy, Oncology Nursing Forum 18 (1991), 1341-1348.
32. J.W. Pennebaker, The Psychology of Physical Symptoms, New York, Springer-Verlag, 1982.
33. L.S. Radloff, The CES-D scale: A self-report depression scale for research in the general population, Applied Psychological Measurement 1 (1977), 385-401.
34. T. D'Zurilla, A.M. Nezu and A. Maydeu-Olivares, Social problem solving: Theory and assessment, in: Social Problem Solving: Theory, Research, and Training, E. Chang, T.J. D'Zurilla and L.J. Sanna, eds, Washington, D.C., American Psychological Association, 2004, pp. 11-27.
35. M.H.L. Lui, F.M. Ross and D.R. Thompson, Supporting family caregivers in stroke care: A review of the evidence for problem solving, Stroke 36 (2005), 2514-2522.
36. A. Nezu, S. Felgoise, K. McClure and P. Houts, Project Genesis: Assessing the efficacy of problem-solving therapy for distressed adult cancer patients, Journal of Consulting and Clinical Psychology 71 (2003), 1037-1048.