Personal and familial predictors of depressive feelings in people with orthopedic disability

Autor

  • Ekin Secinti Indiana University-Purdue University Indianapolis
  • Bilge Selcuk Koç University
  • Mehmet Harma Kadir Has University

Słowa kluczowe:

orthopedic disability, depression, acceptance of disability, family caregiver, social support

Abstrakt

Background

People with orthopedic disability experience limitations in physical ability, which can cause psychological problems such as depressive feelings. This paper investigates the role of family environment, caregiver characteristics, and personal resources in the acceptance of disability and depressive feelings of persons with orthopedic disability.

Participants and procedure

Data were collected from 161 Turkish people with orthopedic disability (mean age = 35.60 years, SD = 10.18) and their family caregivers (e.g., parent, spouse). The participants with disability completed scales for functional independence, acceptance of disability, family environment, locus of control, learned resourcefulness, and depression. The family caregivers completed measures of social support, their own depression, burden of caregiving, and acceptance-rejection of their care recipient.

Results

Analyses via multivariate statistics and SEM showed that depressive feelings of individuals with orthopedic disability and their acceptance of the disability were predicted by multiple factors, including the affected persons’ learned resourcefulness and locus of control, family environment, and interactions with their family caregiver, but not by their functional independence.

Conclusions

Overall, a supportive family environment and acceptance of disability appear to lower the risk of having depression for individuals with orthopedic disability. Family caregivers’ attitudes towards their care recipients were related to the family environment, and feelings of burden appeared to impair the affected individuals’ acceptance of their condition.

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Bibliografia

Anjel, M. (1993). The transliteral equivalence, reliability and validity studies of the Parental Acceptance- Rejection Questionnaire (PARQ) Mother-Form: A tool for assessing child abuse. Istanbul: Bogazici University School of Social Sciences.

Attawong, T., & Kovindha, A. (2005). The influencing factors of acceptance of disability in spinal cord injured patients. Nepal Journal of Neuroscience, 2, 67–70.

Aydemir, O., Suculluoglu Dikici, D., Akdeniz, F., & Kalayci, F. (2012). Reliability and validity of the Turkish version of the Burden Assessment Scale. Archives of Neuropsychiatry, 49, 276–280. doi: 10.4274/npa.y6179

Baydogan, M., & Dag, I. (2008). Prediction of depressiveness by locus of control, learned resourcefulness and sociotropy-autonomy in hemodialysis patients. Turkish Journal of Psychiatry, 19, 19–28.

Beck, A. T., Ward, C. H., Mendelson, M., Mock, J., & Erbaugh, J. (1961). An inventory for measuring depression. Achieves of General Psychiatry, 4, 561–571.

Beedie, A., & Kennedy, P. (2002). Quality of social support predicts hopelessness and depression post spinal cord injury. Journal of Clinical Psychology in Medical Settings, 9, 227–234. doi: 10.1023/A:1016003428370

Bellin, M. H., Zabel, T. A., Dicianno, B. E., Levey, E., Garver, K., Linroth, R., & Braun, P. (2010). Correlates relates of depressive and anxiety symptoms in young adults with spina bifida. Journal of Pediatric Psychology, 35, 778–789. doi: 10.1093/jpepsy/jsp094

Benassi, V. A., Sweeney, P. D., & Dufour, C. L. (1988). Is there a relation between locus of control orientation and depression? Journal of Abnormal Psychology, 97, 357–367. doi: 10.1037/0021-843X.97.3.357

Budh, C. N., & Osteraker, A. L. (2007). Life satisfaction in individuals with a spinal cord injury and pain. Clinical Rehabilitation, 21, 89–96. doi: 10.1177/0269215506070313

Cavallo, S., Feldman, D. E., Swaine, B., & Meshefedjian, G. (2008). Is parental coping associated with the level of function in children with physical disabilities? Child: Care, Health and Development, 35, 33–40. doi: 10.1111/j.1365-2214.2008.00884.x

Chan, R. C. K., Lee, P. W. H., & Lieh-Mak, F. (2000). Coping with spinal cord injury: personal and marital adjustment in the Hong Kong Chinese setting. Spinal Cord, 38, 687–696. doi: 10.1023/A:1016003428370

Craig, A., Tran, Y., & Middleton, J. (2009). Psychological morbidity and spinal cord injury: A systematic review. Spinal Cord, 47, 108–114. doi: 10.1038/sc.2008.115

Crichlow, R. J., Andres, P. L., Morrison, S. M., Haley, S. M., & Vrahas, M. S. (2006). Depression in orthopaedic trauma patients, prevalence and severity. Journal of Bone and Joint Surgery, American Volume, 88, 1927–1933. doi: 10.2106/JBJS.D.02604

Dag, I. (2002). Locus of Control Scale: Scale development, reliability and validity study. Turkish Journal of Psychology, 17, 77–90.

DeLongis, A., & Holzman, S. (2005). Coping in context: The role of stress, social support, and personality in coping. Journal of Personality, 73, 1–24. doi: 10.1111/j.1467-6494.2005.00361.x

DeVivo, M. J., Black, K. J., Richards, J. S., & Stover, S. L. (1991). Suicide following spinal cord injury. Paraplegia 29, 620–627. doi: 10.1038/sc.1991.91

Donelan, K., Hill, C. A., Hoffman, C., Scoles, K., Hoffman, P. H., Levine, C., & Gould, D. (2002). Challenged to care: Informal caregivers in a changing spinal cord injury. Health Affairs, 21, 222–231. doi: 10.1377/hlthaff.21.4.222

Dreer, L. E., Elliott, T. R., Shewchuk, R., Berry, J. W., & Rivera, P. (2007). Family caregivers of persons with spinal cord injury: predicting caregivers at risk for probable depression. Rehabilitation Psychology, 52, 351–357. doi: 10.1037/0090-5550.52.3.351

Drummond-Young, M., LeGris, J., Browne, G., Pallister, R., & Roberts, J. (1995). Interactional styles of out-patients with poor adjustment to chronić illness receiving problem-solving counselling. Health and Social Care in the Community, 4, 317–329. doi: 10.1111/j.1365-2524.1996.tb00078.x

Elfstrom, M., Kreuter, M., Ryden, A., Persson, L. O., & Sullivan, M. (2002). Effects of coping on psychological outcome when controlling for background variables: a study of traumatically spinal cord lesioned persons focus on coping. Spinal Cord, 40, 408–415. doi: 10.1080/16501970410034414

Elliott, T. R., & Berry, J. W. (2009). Brief problem solving training for family caregivers of persons with recent onset spinal cord injuries: a randomized controlled trial. Journal of Clinical Psychology, 65, 406–422. doi: 10.1002/jclp.20527

Elliott, T. R., & Pezent, G. D. (2008). Family caregivers of older persons in rehabilitation. Neurorehabilitation, 23, 1–8.

Elliott, T. R. (1999). Social problem-solving abilities and adjustment to recent onset spinal cord injury. Rehabilitation Psychology, 44, 315–332. doi: 10.1037/0090-5550.44.4.315

Elliott, T. R., Uswatte, G., Lewis, L., & Palmatier, A. (2000). Goal instability and adjustment to physical disability. Journal of Counseling Psychology, 47, 251–265. doi: 10.1037/0022-0167.47.2.251

Epstein, N. B., Baldwin, L. M., & Bishop D. S. (1983). The McMaster Family Assessment Device. Journal of Marital and Family Therapy, 9, 171–180. doi: 10.1111/j.1752-0606.1983.tb01497.x

Fekete, C., Eriks-Hooglans, I., Baumberger, M., Catz, A., Itzkovich, M., Luthi, H., Post, M. W., von Elm, E., Wyss, A., & Brinkhof, M. W. (2013). Development and validation of a self-report version of the spinal cord independence measure (SCIM III). Spinal Cord, 40, 40–47. doi: 10.1038/sc.2012.87

Green, B., Pratt, C., & Grigsby, T. (1984). Self-concept among persons with long-term spinal cord injury. Archives of Physical Medicine and Rehabilitation, 65, 751–754.

Groomes, D. A. G., & Linkowski, D. C. (2007). Examining the Structure of the Revised Acceptance Disability Scale. Journal of Rehabilitation, 73, 3–9.

Gunes, Z., & Oner, H. (2009). Relationship between hopelessness and perceived social support from family patients who has chronic illness. Journal of Istanbul University Florence Nightingale School of Nursing, 17, 16–23.

Henderson, S., Duncan-Jones, P., McAuley H., & Ritchie, K. (1978). The patient’s primary group. British Journal of Psychiatry, 132, 74–86.

Huang, C. Y., Guo, S. E., Hung, C. M., Shih, S. L., Lee, L. C., Hung, G. C., & Huang, S. M. (2010). Learned resourcefulness, quality of life and depressive symptoms for patients with breast cancer. Oncology Nursing Forum, 37, 280–287. doi: 10.1188/10.ONF.E280-E287

Jiao, J., Heyne, M. M., & Lam, C. S. (2012). Acceptance of disability among Chinese individuals with spinal cord injuries: the effects of social support and depression. Psychology, 3, 775–781. doi: 10.4236/psyc.2012.329117

Kahan, J., Mitchell, J., Kemp, B., & Adkins, R. H. (2006). The results of a 6-month treatment for depression on symptoms, life satisfaction, and community activities among individuals aging with a disability. Rehabilitation Psychology, 51, 13–22. doi: 10.1037/0090-5550.51.1.13

Keany, K. C., & Glueckauf, R. L. (1993). Disability and value change: an overview and reanalysis of acceptance of loss theory. Rehabilitation Psychology, 38, 199–210. doi: 10.1037/h0080297

Kemp, B. J, & Krause, J. S. (1999). Depression and life satisfaction among people ageing with post-polio and spinal cord injury. Disability and Rehabilitation, 21, 241–249. doi: 10.1080/096382899297666

Kendall, E., & Buys, N. (1998). An integrated model of psychosocial adjustment following acquired disability. Journal of Rehabilitation, 64, 16–20.

Kennedy, P., Duff, J., Evans, M., & Beedie, A. (2003). Coping effectiveness training reduces depression and anxiety following traumatic spinal cord injuries. British Journal of Clinical Psychology, 42, 41–52. doi: 10.1348/014466503762842002.

Kesiktas, N., Paker, N., Bugdayci, D., Sencan, S., Karan A., & Muslumanoglu, L. (2011). Turkish adaptation of Spinal Cord Independence Measure – Version III. International Journal of Rehabilitation Research, 35, 88–91. doi: 10.1097/MRR.0b013e32834f402d

Kim, E. (2011). Korean American parental depressive symptoms and parental acceptance-rejection and control. Issues in Mental Health Nursing, 32, 114–120. doi: 10.3109/01612840.2010.529239

Kishi, Y., & Robinson, R. G. (1996). Suicidal plans following spinal cord injury. Journal of Neuropsychiatry, 8, 443–445.

Krause, J. S., Sternberg, M., Lottes, S., & Maides, J. (1997). Mortality after spinal cord injury: an 11- year prospective study. Archives of Physical Medicine and Rehabilitation, 78, 815–821. doi: 10.1016/S0003-9993(97)90193-3

Li, L., & Moore, D. (1998). Acceptance of disability and its correlates. The Journal of Social Psychology, 138, 13–25. doi: 10.1080/00224549809600349

McCartney, K. K., Burchinal, M. R., & Bub, K. L. (2006). Best practices in quantitative methods for developmentalists. Monographs of The Society For Research In Child Development, 71, 1–145. doi: 10.1111/j.1540-5834.2006.07103001.x

Melamed, S., Groswasser, Z., & Stem, M. J. (1992). Acceptance of disability, work involvement and subjective rehabilitation status of traumatic brain-injured (TBI) patients. Brain Injury, 6, 233–243. doi: 10.3109/02699059209029665

Moroni, L., Colangelo, M., Gallì, M., & Bertolotti, G. (2007). “I would like to give him my life”: Results of a psychological support intervention to caregivers of patients undergoing neuromotor rehabilitation. Italian Journal of Occupational Medicine and Ergonomics, 29, 5–17.

Müller, R., Peter, C., Cieza, A., & Geyh, S. (2012). The role of social support and social skills in people with spinal cord injury – A systematic review of the literature. Spinal Cord, 50, 94–106. doi: 10.1038/sc.2011.116

Oh, H., & Lee, E. O. (2009). Caregiver burden and social support among mothers raising children with developmental disabilities in South Korea. International Journal of Disability, 56, 149–167. doi: 10.1080/10349120902868624

Ozgul, A., Yazicioglu, K., Peker, F., Taskaynatan, M. A., & Kalyon, T. A. (2003). The study of the familial functions of married paraplegic patients. Turkish Journal of Physical Medicine and Rehabilitation, 49, 3–7.

Pelletier, P. M., Alfano, D. P., & Fink, M. P. (1994). Social support, locus of control and psychological health in family members following head or spinal cord injury. Applied Neuropsychology, 1, 38–44. doi: 10.1080/09084282.1994.9645329

Pierangelo, R., & Giuliani, G. (2007). The educator’s manual of disabilities and disorders. San Francisco, CA: Wiley.

Post, M. W., & van Leeuwen, C. M. (2012). Psychosocial issues in spinal cord injury: a review. Spinal Cord, 50, 382–389. doi: 10.1038/sc.2011.182

Procidano, M. E., & Heller, K. (1983). Measures of perceived social support from friends and from family: Three validation studies. American Journal of Community Psychology, 11, 1–24. doi: 10.1007/BF00898416

Reinhard, S. C., Gubman, G. D., Horwitz, A. V., & Minsky, S. (1994). Burden Assessment Scale for families of the seriously mentally ill. Evaluation and Program Planning, 17, 261–269. doi: 10.1016/0149-7189(94)90004-3

Rintala, D. H., Robinson-Whelen, S., & Matamoros, R. (2005). Subjective stress in male veterans with spinal cord injury. Journal of Rehabilitation Research and Development, 42, 291–304. doi: 10.1682/JRRD.2005.10.0155

Robinson-Whelen, S., & Rintala, D. H. (2003). Informal care providers for veterans with SCI: who are they and how are they doing? Journal of Rehabilitation Research and Development, 40, 511–516.

Rodgers, M. L., Strode, A. D., Norell, D. M., Short, R. A., Dyck, D. G., & Becker, B. (2007). Adapting multiple-family group treatment for brain and spinal cord injury intervention development preliminary outcomes. American Journal of Physical Medicine & Rehabilitation, 86, 482–492. doi: 10.1097/PHM.0b013e31805c00a1

Rohner, R. P., & Rohner, E. C. (1980). Worldwide tests of parental acceptance-rejection theory. Behavioral Science Research, 15, 1–21.

Rosenbaum, M. (1990). The role of learned resourcefulness in the self-control of health behavior. In M. Rosenbaum (ed.), Learned resourcefulness On coping skills, self-control, and adaptive behawior (pp. 3–29). New York, NY: Springer.

Rosenbaum, M. (1980). A schedule for assessing self-controlling behaviors: Preliminary findings. Behavior Therapy, 11, 109–121.

Rosenbaum, M., & Palmon, N. (1984). Helplessness and resourcefulness in coping with epilepsy. Journal of Consulting and Clinical Psychology, 52, 244–253. doi: 10.1016/S0005-7894(80)80040-2

Rotter, J. B. (1966). Generalized expectancies for internal versus external control of reinforcement. Psychological Monographs, 80 (1, Whole No. 609). doi: 10.1037/h0092976

Russell, D., Turner, R. J., & Joiner, T. E. (2009). Physical disability and suicidal ideation: a community- based study of risk/protective factors for suicidal thoughts. Suicide and Life Threatening Behavior, 39, 440–451. doi: 10.1521/suli.2009.39.4.440

Sav, A., Kendall, E., McMillan, S., Kelly, F., Whitty, J. A., King, M. A., & Wheeler, A. J. (2013). ‘You say treatment, I say hard work’: treatment burden among people with chronic illness and their carers in Australia. Health and Social Care in the Community, 21, 665–674. doi: 10.1111/hsc.12052

Singh, R., Ripley, D., Pentland, B., Todd, I., Hunter, J., Hutton, L., & Philip, A. (2009). Depression and anxiety symptoms after lower limb amputation: the rise and fall. Clinical Rehabilitation, 23, 281– 286. doi: 10.1177/0269215508094710

Snead, S. L., & Davis, J. R. (2002). Attitudes of individuals with acquired brain injury towards disability. Brain Injury, 16, 947–953. doi: 10.1080/02699050210147211

Turkish Statistical Institute (2010). Survey on Problems and Expectations of Disabled People. Retrieved from http://www.tuik.gov.tr

Unalan, H., Gencosmanoglu, B., Akgun, K., Karamehmetoglu, S., Tuna, H., Ones, K., Rahimpenah, A., Uzun, E., & Tüzün, F. (2001). Quality of life of primary caregivers of spinal cord injury survivors living in the community: Controlled study with short form-36 questionnaire. Spinal Cord, 39, 318–322. doi: 10.1038/sj.sc.3101163

Van Leeuwen, C. M., Kraaijeveld, S., Lindeman, E., & Post, M. W. (2012). Associations between psychological factors and quality of life ratings in persons with spinal cord injury: a systematic review. Spinal Cord, 50, 174–187. doi: 10.1038/sc.2011.120

Vitaliano, P. P., Zhang, J., & Scanlan, J. (2003). Is caregiving hazardous to one’s physical health? A meta- analysis. Psychological Bulletin, 129, 946–972. doi: 10.1037/00332909.129.6.946

Waldron, B., Benson, C., O’Connell, A., Byrne, P., Dooley, B., & Burke, T. (2010). Health locus of control and attributions of cause and blame in adjustment to spinal cord injury. Spinal Cord, 48, 598–602. doi: 10.1038/sc.2009.182

Weitzenkamp, D., Gerhart, K. A., Charlifue, S. W., & Whiteneck, G. G. (1997). Spouses of spinal cord injured survivors: the added impact of caregiving. Archives of Physical Medicine and Rehabilitation, 78, 822–827. doi: 10.1016/S0003-9993(97)90194-5

Williams, A. M., Wang, L., & Kitchen, P. (2016). Impacts of care-giving and sources of support: a comparison of end-of-life and non-end-of-life caregivers in Canada. Health & Social Care in the Community, 24, 214–224. doi: 10.1111/hsc.12205

Woodrich, F., & Petterson, J. B. (1983). Variables related to acceptance of disability in persons with spinal cord injuries. Journal of Rehabilitation, 49, 26–30.

Yagmurlu, M. F., Yagmurlu, B., & Yilmaz, M. (2009). Orthopedic disability and socioemotional functioning. Pediatrics International, 51, 637–644. doi: 10.1111/j.1442-200X.2009.02821.x

Yagmurlu, B., Yavuz, H. M., & Sen, H. (2015). Well-being of mothers of children with orthopedic disabilities in a disadvantaged context: findings from Turkey. Journal of Child and Family Studies, 24, 948–956. doi: 10.1007/s10826-014-9905-8

Ylven, R., Bjorck-Akesson, E., & Granlund, M. (2006). Literature review of positive functioning in families with children with a disability. Journal of Policy and Practice in Intellectual Disabilities, 3, 253–270. doi: 10.1111/j.1741-1130.2006.00089.x

Zimet, G. D., Dahlem, N. W., Zimet, S. G., & Farley, G. K. (1988). The Multidimensional Scale of Perceived Social Support. Journal of Personality Assessment, 52, 30–41. doi: 10.1207/s15327752jpa5201_2

Opublikowane

2017-09-25

Jak cytować

Secinti, E., Selcuk, B., & Harma, M. (2017). Personal and familial predictors of depressive feelings in people with orthopedic disability. Health Psychology Report, 5(3), 227–239. Pobrano z https://czasopisma.bg.ug.edu.pl/index.php/HPR/article/view/9154

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