An App-Based Just-in-Time Adaptive Self-management Intervention for Care Partners (CareQOL): Protocol for a Pilot Trial

Noelle E Carlozzi, Sung Won Choi, Zhenke Wu, Jennifer A Miner, Angela K Lyden, Christopher Graves, Jitao Wang, Srijan Sen, Noelle E Carlozzi, Sung Won Choi, Zhenke Wu, Jennifer A Miner, Angela K Lyden, Christopher Graves, Jitao Wang, Srijan Sen

Abstract

Background: Care partners (ie, informal family caregivers) of individuals with health problems face considerable physical and emotional stress, often with a substantial negative impact on the health-related quality of life (HRQOL) of both care partners and care recipients. Given that these individuals are often overwhelmed by their caregiving responsibilities, low-burden self-management interventions are needed to support care partners to ensure better patient outcomes.

Objective: The primary objective of this study is to describe an intensive data collection protocol that involves the delivery of a personalized just-in-time adaptive intervention that incorporates passive mobile sensor data feedback (sleep and activity data from a Fitbit [Fitbit LLC]) and real time self-reporting of HRQOL via a study-specific app called CareQOL (University of Michigan) to provide personalized feedback via app alerts.

Methods: Participants from 3 diverse care partner groups will be enrolled (care partners of persons with spinal cord injury, care partners of persons with Huntington disease, and care partners of persons with hematopoietic cell transplantation). Participants will be randomized to either a control group, where they will wear the Fitbit and provide daily reports of HRQOL over a 3-month (ie, 90 days) period (without personalized feedback), or the just-in-time adaptive intervention group, where they will wear the Fitbit, provide daily reports of HRQOL, and receive personalized push notifications for 3 months. At the end of the study, participants will complete a feasibility and acceptability questionnaire, and metrics regarding adherence and attrition will be calculated.

Results: This trial opened for recruitment in November 2020. Data collection was completed in June 2021, and the primary results are expected to be published in 2022.

Conclusions: This trial will determine the feasibility and acceptability of an intensive app-based intervention in 3 distinct care partner groups: care partners for persons with a chronic condition that was caused by a traumatic event (ie, spinal cord injury); care partners for persons with a progressive, fatal neurodegenerative disease (ie, Huntington disease); and care partners for persons with episodic cancer conditions that require intense, prolonged inpatient and outpatient treatment (persons with hematopoietic cell transplantation).

Trial registration: ClinicalTrials.gov NCT04556591; https://ichgcp.net/clinical-trials-registry/NCT04556591.

International registered report identifier (irrid): DERR1-10.2196/32842.

Keywords: Huntington disease; caregivers; feasibility studies; hematopoietic stem cell transplantation; mobile apps; mobile phone; outcome assessment; quality of life; self-management; spinal cord injuries.

Conflict of interest statement

Conflicts of Interest: None declared.

©Noelle E Carlozzi, Sung Won Choi, Zhenke Wu, Jennifer A Miner, Angela K Lyden, Christopher Graves, Jitao Wang, Srijan Sen. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 09.12.2021.

Figures

Figure 1
Figure 1
Screenshots of the CareQOL app.

References

    1. Kreutzer JS, Gervasio AH, Camplair PS. Primary caregivers' psychological status and family functioning after traumatic brain injury. Brain Inj. 1994 Apr 03;8(3):197–210. doi: 10.3109/02699059409150973.
    1. Hall KM, Karzmark P, Stevens M, Englander J, O'Hare P, Wright J. Family stressors in traumatic brain injury: a two-year follow-up. Arch Phys Med Rehabil. 1994 Aug;75(8):876–84. doi: 10.1016/0003-9993(94)90112-0.0003-9993(94)90112-0
    1. Panting A, Merry P. The long term rehabilitation of severe head injuries with particular reference to the need for social and medical support for the patient's family. Rehabilitation. 1972;38:33–7.
    1. Marsh NV, Kersel DA, Havill JH, Sleigh JW. Caregiver burden at 6 months following severe traumatic brain injury. Brain Inj. 1998 Mar 03;12(3):225–38. doi: 10.1080/026990598122700.
    1. Livingston MG, Brooks DN, Bond MR. Patient outcome in the year following severe head injury and relatives' psychiatric and social functioning. J Neurol Neurosurg Psychiatry. 1985 Sep 01;48(9):876–81. doi: 10.1136/jnnp.48.9.876.
    1. Saban KL, Griffin JM, Urban A, Janusek MA, Pape TL, Collins E. Perceived health, caregiver burden, and quality of life in women partners providing care to Veterans with traumatic brain injury. J Rehabil Res Dev. 2016;53(6):681–692. doi: 10.1682/JRRD.2015.07.0143. JRRD-2015-07-0143
    1. Carlozzi NE, Brickell TA, French LM, Sander A, Kratz AL, Tulsky DS, Chiaravalloti ND, Hahn EA, Kallen M, Austin AM, Miner JA, Lange RT. Caring for our wounded warriors: A qualitative examination of health-related quality of life in caregivers of individuals with military-related traumatic brain injury. J Rehabil Res Dev. 2016;53(6):669–680. doi: 10.1682/JRRD.2015.07.0136. JRRD-2015-07-0136
    1. Knight RG, Devereux R, Godfrey HP. Caring for a family member with a traumatic brain injury. Brain Inj. 1998 Jul 03;12(6):467–81. doi: 10.1080/026990598122430.
    1. Marsh NV, Kersel DA, Havill JH, Sleigh JW. Caregiver burden during the year following severe traumatic brain injury. J Clin Exp Neuropsychol. 2002 Jun 09;24(4):434–47. doi: 10.1076/jcen.24.4.434.1030.
    1. Arango-Lasprilla J, Nicholls E, Cabrera TV, Drew A, Jimenez-Maldonado M, Martinez-Cortes M. Health-related quality of life in caregivers of individuals with traumatic brain injury from Guadalajara, Mexico. J Rehabil Med. 2011 Nov;43(11):983–6. doi: 10.2340/16501977-0883.
    1. McPherson K, Pentland B, McNaughton H. Brain injury - the perceived health of carers. Disabil Rehabil. 2000 Oct 15;22(15):683–9. doi: 10.1080/096382800445489.
    1. Morin CM, Culbert JP, Schwartz SM. Nonpharmacological interventions for insomnia: a meta-analysis of treatment efficacy. Am J Psychiatry. 1994 Aug;151(8):1172–80. doi: 10.1176/ajp.151.8.1172.
    1. Montgomery P, Dennis J. Cognitive behavioural interventions for sleep problems in adults aged 60+ Cochrane Database Syst Rev. 2003;(1):CD003161. doi: 10.1002/14651858.CD003161.
    1. Carlozzi NE, Kratz AL, Sander AM, Chiaravalloti ND, Brickell TA, Lange RT, Hahn EA, Austin A, Miner JA, Tulsky DS. Health-related quality of life in caregivers of individuals with traumatic brain injury: development of a conceptual model. Arch Phys Med Rehabil. 2015 Jan;96(1):105–13. doi: 10.1016/j.apmr.2014.08.021. S0003-9993(14)01035-1
    1. Ponsford J, Schönberger Michael. Family functioning and emotional state two and five years after traumatic brain injury. J Int Neuropsychol Soc. 2010 Mar;16(2):306–17. doi: 10.1017/S1355617709991342.S1355617709991342
    1. Brooks N, Campsie L, Symington C, Beattie A, McKinlay W. The five year outcome of severe blunt head injury: a relative's view. J Neurol Neurosurg Psychiatry. 1986 Jul 01;49(7):764–70. doi: 10.1136/jnnp.49.7.764.
    1. Brooks N, Campsie L, Symington C, Beattie A, McKinlay W. The effects of severe head injury on patient and relative within seven years of injury. J Head Trauma Rehabil. 1987;2(3):1–13. doi: 10.1097/00001199-198709000-00003.
    1. Kreutzer JS, Rapport LJ, Marwitz JH, Harrison-Felix C, Hart T, Glenn M, Hammond F. Caregivers' well-being after traumatic brain injury: a multicenter prospective investigation. Arch Phys Med Rehabil. 2009 Jun;90(6):939–46. doi: 10.1016/j.apmr.2009.01.010.S0003-9993(09)00202-0
    1. Gillen R, Tennen H, Affleck G, Steinpreis R. Distress, depressive symptoms, and depressive disorder among caregivers of patients with brain injury. J Head Trauma Rehabil. 1998 Jun;13(3):31–43. doi: 10.1097/00001199-199806000-00004.
    1. Winstanley J, Simpson G, Tate R, Myles B. Early indicators and contributors to psychological distress in relatives during rehabilitation following severe traumatic brain injury: findings from the Brain Injury Outcomes Study. J Head Trauma Rehabil. 2006;21(6):453–66. doi: 10.1097/00001199-200611000-00001.00001199-200611000-00001
    1. Pickett T, Altmaier E, Paulsen JS. Caregiver burden in Huntington's disease. Rehabil Psychol. 2007;52(3):311–8. doi: 10.1037/0090-5550.52.3.311.
    1. Bevans MF, Mitchell SA, Marden S. The symptom experience in the first 100 days following allogeneic hematopoietic stem cell transplantation (HSCT) Support Care Cancer. 2008 Nov 6;16(11):1243–54. doi: 10.1007/s00520-008-0420-6.
    1. Simoneau TL, Mikulich-Gilbertson SK, Natvig C, Kilbourn K, Spradley J, Grzywa-Cobb R, Philips S, McSweeney P, Laudenslager ML. Elevated peri-transplant distress in caregivers of allogeneic blood or marrow transplant patients. Psychooncology. 2013 Sep 25;22(9):2064–70. doi: 10.1002/pon.3259.
    1. Applebaum AJ, Bevans M, Son T, Evans K, Hernandez M, Giralt S, DuHamel K. A scoping review of caregiver burden during allogeneic HSCT: lessons learned and future directions. Bone Marrow Transplant. 2016 Nov 13;51(11):1416–22. doi: 10.1038/bmt.2016.164. bmt2016164
    1. Foxall MJ, Gaston-Johansson F. Burden and health outcomes of family caregivers of hospitalized bone marrow transplant patients. J Adv Nurs. 1996 Nov;24(5):915–23. doi: 10.1111/j.1365-2648.1996.tb02926.x.
    1. Jumisko E, Lexell J, Söderberg S. Living with moderate or severe traumatic brain injury: the meaning of family members' experiences. J Fam Nurs. 2007 Aug 24;13(3):353–69. doi: 10.1177/1074840707303842.13/3/353
    1. Peters LC, Stambrook M, Moore AD, Esses L. Psychosocial sequelae of closed head injury: effects on the marital relationship. Brain Inj. 1990 Jul 03;4(1):39–47. doi: 10.3109/02699059009026147.
    1. Wood RL, Yurdakul LK. Change in relationship status following traumatic brain injury. Brain Inj. 1997 Jul;11(7):491–501.
    1. Kozloff R. Networks of social support and the outcome from severe head injury. J Head Trauma Rehabil. 1987;2(3):14–23. doi: 10.1097/00001199-198709000-00004.
    1. Caregivers of Veterans – serving on the homefront : report of study findings. National Alliance for Caregiving. 2010. [2021-11-08]. .
    1. Lester P, Peterson K, Reeves J, Knauss L, Glover D, Mogil C, Duan N, Saltzman W, Pynoos R, Wilt K, Beardslee W. The long war and parental combat deployment: effects on military children and at-home spouses. J Am Acad Child Adolesc Psychiatry. 2010 Apr;49(4):310–20. S0890-8567(10)00077-8
    1. Ruff RL, Ruff SS, Wang X. Improving sleep: initial headache treatment in OIF/OEF veterans with blast-induced mild traumatic brain injury. J Rehabil Res Dev. 2009;46(9):1071–84. doi: 10.1682/jrrd.2009.05.0062.
    1. Taft CT, Schumm JA, Panuzio J, Proctor SP. An examination of family adjustment among Operation Desert Storm veterans. J Consult Clin Psychol. 2008 Aug;76(4):648–56. doi: 10.1037/a0012576.2008-09736-010
    1. Mansfield AJ, Kaufman JS, Marshall SW, Gaynes BN, Morrissey JP, Engel CC. Deployment and the use of mental health services among U.S. Army wives. N Engl J Med. 2010 Jan 14;362(2):101–9. doi: 10.1056/NEJMoa0900177.362/2/101
    1. Jacobs HE. The Los Angeles Head Injury Survey: procedures and initial findings. Arch Phys Med Rehabil. 1988 Jun;69(6):425–31.
    1. McCabe MP, Firth L, O'Connor Elodie. A comparison of mood and quality of life among people with progressive neurological illnesses and their caregivers. J Clin Psychol Med Settings. 2009 Dec 29;16(4):355–62. doi: 10.1007/s10880-009-9168-5.
    1. O'Connor EJ, McCabe MP. Predictors of quality of life in carers for people with a progressive neurological illness: a longitudinal study. Qual Life Res. 2011 Jun 2;20(5):703–11. doi: 10.1007/s11136-010-9804-4.
    1. Roscoe LA, Corsentino E, Watkins S, McCall M, Sanchez-Ramos J. Well-being of family caregivers of persons with late-stage Huntington's disease: lessons in stress and coping. Health Commun. 2009 Apr 08;24(3):239–48. doi: 10.1080/10410230902804133.910939997
    1. Aubeeluck A. Caring for the carers: quality of life in Huntington's disease. Br J Nurs. 2005 Apr;14(8):452–4. doi: 10.12968/bjon.2005.14.8.17929.
    1. Aubeeluck AV, Buchanan H, Stupple EJ. 'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients. Qual Life Res. 2012 Oct 13;21(8):1425–35. doi: 10.1007/s11136-011-0062-x.
    1. Cox M. Quality of life among carers of people with Huntington’s disease. Br J Neurosci Nurs. 2012 Oct;8(5):288–94. doi: 10.12968/bjnn.2012.8.5.288.
    1. Northouse LL, Katapodi MC, Schafenacker AM, Weiss D. The impact of caregiving on the psychological well-being of family caregivers and cancer patients. Semin Oncol Nurs. 2012 Nov;28(4):236–45. doi: 10.1016/j.soncn.2012.09.006. S0749-2081(12)00057-5
    1. Bevans M, Sternberg EM. Caregiving burden, stress, and health effects among family caregivers of adult cancer patients. J Am Med Assoc. 2012 Jan 25;307(4):398–403. doi: 10.1001/jama.2012.29. 307/4/398
    1. Stenberg U, Ruland CM, Miaskowski C. Review of the literature on the effects of caring for a patient with cancer. Psychooncology. 2010 Oct 14;19(10):1013–25. doi: 10.1002/pon.1670.
    1. Ready RE, Mathews M, Leserman A, Paulsen JS. Patient and caregiver quality of life in Huntington's disease. Mov Disord. 2008 Apr 15;23(5):721–6. doi: 10.1002/mds.21920.
    1. Anderson VA, Catroppa C, Haritou F, Morse S, Pentland L, Rosenfeld J, Stargatt R. Predictors of acute child and family outcome following traumatic brain injury in children. Pediatr Neurosurg. 2001 Mar 2;34(3):138–48. doi: 10.1159/000056009.56009
    1. Sander AM, Caroselli JS, High WM, Becker C, Neese L, Scheibel R. Relationship of family functioning to progress in a post-acute rehabilitation programme following traumatic brain injury. Brain Inj. 2002 Aug 03;16(8):649–57. doi: 10.1080/02699050210128889.
    1. Temple JL, Struchen MA, Pappadis MR. Impact of pre-injury family functioning and resources on self-reported post-concussive symptoms and functional outcomes in persons with mild TBI. Brain Inj. 2016 Oct 14;30(13-14):1672–82. doi: 10.3109/02699052.2015.1113561.
    1. Holland JN, Schmidt AT. Static and dynamic factors promoting resilience following traumatic brain injury: a brief review. Neural Plast. 2015;2015:902802. doi: 10.1155/2015/902802. doi: 10.1155/2015/902802.
    1. Schönberger M, Ponsford J, Olver J, Ponsford M. A longitudinal study of family functioning after TBI and relatives' emotional status. Neuropsychol Rehabil. 2010 Dec;20(6):813–29. doi: 10.1080/09602011003620077.927100089
    1. Ramkumar NA, Elliott TR. Family caregiving of persons following neurotrauma: issues in research, service and policy. NeuroRehabilitation. 2010;27(1):105–12. doi: 10.3233/NRE-2010-0585. 87T26269640U2152
    1. Kreutzer J, Marwitz JH, Godwin EE, Arango-Lasprilla JC. Practical approaches to effective family intervention after brain injury. J Head Trauma Rehabil. 2010;25(2):113–20. doi: 10.1097/HTR.0b013e3181cf0712.
    1. Vangel S, Rapport LJ, Hanks RA. Effects of family and caregiver psychosocial functioning on outcomes in persons with traumatic brain injury. J Head Trauma Rehabil. 2011;26(1):20–9. doi: 10.1097/HTR.0b013e318204a70d.00001199-201101000-00003
    1. Sander AM, Maestas KL, Sherer M, Malec JF, Nakase-Richardson R. Relationship of caregiver and family functioning to participation outcomes after postacute rehabilitation for traumatic brain injury: a multicenter investigation. Arch Phys Med Rehabil. 2012 May;93(5):842–8. doi: 10.1016/j.apmr.2011.11.031.S0003-9993(11)01064-1
    1. Smith A, Schwirian PM. The relationship between caregiver burden and TBI survivors' cognition and functional ability after discharge. Rehabil Nurs. 1998;23(5):252–7. doi: 10.1002/j.2048-7940.1998.tb01795.x.
    1. Florian V, Katz S, Lahav V. Impact of traumatic brain damage on family dynamics and functioning: a review. Brain Inj. 1989 Jul 03;3(3):219–33. doi: 10.3109/02699058909029637.
    1. McLaughlin A, Carey JL. The adversarial alliance: developing therapeutic relationships between families and the team in brain injury rehabilitation. Brain Inj. 1993 Jul 03;7(1):45–51. doi: 10.3109/02699059309008155.
    1. Pelletier P, Alfano D. Depression, social support, and family coping following traumatic brain injury. Brain Cogn. 2000 Oct;44(1):45–9. doi: 10.1016/s0278-2626(20)30187-1.
    1. Sady MD, Sander AM, Clark AN, Sherer M, Nakase-Richardson R, Malec JF. Relationship of preinjury caregiver and family functioning to community integration in adults with traumatic brain injury. Arch Phys Med Rehabil. 2010 Oct;91(10):1542–50. doi: 10.1016/j.apmr.2010.07.012.S0003-9993(10)00393-X
    1. Barata A, Wood WA, Choi SW, Jim HS. Unmet needs for psychosocial care in hematologic malignancies and hematopoietic cell transplant. Curr Hematol Malig Rep. 2016 Aug 25;11(4):280–7. doi: 10.1007/s11899-016-0328-z.10.1007/s11899-016-0328-z
    1. Rohleder N, Marin TJ, Ma R, Miller GE. Biologic cost of caring for a cancer patient: dysregulation of pro- and anti-inflammatory signaling pathways. J Clin Oncol. 2009 Jun 20;27(18):2909–15. doi: 10.1200/JCO.2008.18.7435.JCO.2008.18.7435
    1. Shaffer KM, Kim Y, Carver CS, Cannady RS. Effects of caregiving status and changes in depressive symptoms on development of physical morbidity among long-term cancer caregivers. Health Psychol. 2017 Aug;36(8):770–8. doi: 10.1037/hea0000528. 2017-27047-001
    1. Kent EE, Rowland JH, Northouse L, Litzelman K, Chou WS, Shelburne N, Timura C, O'Mara A, Huss K. Caring for caregivers and patients: research and clinical priorities for informal cancer caregiving. Cancer. 2016 Jul 01;122(13):1987–95. doi: 10.1002/cncr.29939. doi: 10.1002/cncr.29939.
    1. Cancer caregiving in the U. S.: an intense, episodic, and challenging care experience. National Alliance for Caregiving, in partnership with the National Cancer Institute and the Cancer Support Community. 2016. [2021-10-27]. .
    1. Hurria A, Naylor M, Cohen HJ. Improving the quality of cancer care in an aging population: recommendations from an IOM report. J Am Med Assoc. 2013 Nov 06;310(17):1795–6. doi: 10.1001/jama.2013.280416.1764058
    1. Cotner B, Carlozzi N, Lange R, Louis F, O’Connor D, Nakase-Richardson R, Brickell T. Quality of sleep in caregivers of service members and veterans with traumatic brain injury. Arch Phys Med Rehabil. 2017 Oct;98(10):97–8. doi: 10.1016/j.apmr.2017.08.314.
    1. Johnson MD, Contrino A, Contrino J, Maxwell K, Leonard G, Kreutzer D. Murine model of otitis media with effusion: immunohistochemical demonstration of IL-1 alpha antigen expression. Laryngoscope. 1994 Sep;104(9):1143–9. doi: 10.1288/00005537-199409000-00016.
    1. Banaszkiewicz K, Sitek EJ, Rudzińska M, Sołtan W, Sławek J, Szczudlik A. Huntington's disease from the patient, caregiver and physician's perspectives: three sides of the same coin? J Neural Transm (Vienna) 2012 Nov 8;119(11):1361–5. doi: 10.1007/s00702-012-0787-x.
    1. Wells R, Dywan J, Dumas J. Life satisfaction and distress in family caregivers as related to specific behavioural changes after traumatic brain injury. Brain Inj. 2005 Dec 03;19(13):1105–15. doi: 10.1080/02699050500150062.W1960167M2278737
    1. Nahum-Shani I, Smith SN, Spring BJ, Collins LM, Witkiewitz K, Tewari A, Murphy SA. Just-in-Time Adaptive Interventions (JITAIs) in Mobile Health: key components and design principles for ongoing health behavior support. Ann Behav Med. 2018 May 18;52(6):446–62. doi: 10.1007/s12160-016-9830-8. 10.1007/s12160-016-9830-8
    1. Nahum-Shani I, Hekler EB, Spruijt-Metz D. Building health behavior models to guide the development of just-in-time adaptive interventions: a pragmatic framework. Health Psychol. 2015 Dec;34S(Suppl):1209–19. doi: 10.1037/hea0000306. 2015-56045-002
    1. Ben-Zeev D, Brenner CJ, Begale M, Duffecy J, Mohr DC, Mueser KT. Feasibility, acceptability, and preliminary efficacy of a smartphone intervention for schizophrenia. Schizophr Bull. 2014 Nov 08;40(6):1244–53. doi: 10.1093/schbul/sbu033. sbu033
    1. Riley W, Obermayer J, Jean-Mary J. Internet and mobile phone text messaging intervention for college smokers. J Am Coll Health. 2008;57(2):245–8. doi: 10.3200/JACH.57.2.245-248.R4883H2681063U21
    1. Free C, Knight R, Robertson S, Whittaker R, Edwards P, Zhou W, Rodgers A, Cairns J, Kenward MG, Roberts I. Smoking cessation support delivered via mobile phone text messaging (txt2stop): a single-blind, randomised trial. Lancet. 2011 Jul 02;378(9785):49–55. doi: 10.1016/S0140-6736(11)60701-0. S0140-6736(11)60701-0
    1. Mirowski M, Reid PR, Mower MM, Watkins L, Gott VL, Schauble JF, Langer A, Heilman MS, Kolenik SA, Fischell RE, Weisfeldt ML. Termination of malignant ventricular arrhythmias with an implanted automatic defibrillator in human beings. N Engl J Med. 1980 Aug 07;303(6):322–4. doi: 10.1056/NEJM198008073030607.
    1. Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group. Tamborlane WV, Beck RW, Bode BW, Buckingham B, Chase HP, Clemons R, Fiallo-Scharer R, Fox LA, Gilliam LK, Hirsch IB, Huang ES, Kollman C, Kowalski AJ, Laffel L, Lawrence JM, Lee J, Mauras N, O'Grady M, Ruedy KJ, Tansey M, Tsalikian E, Weinzimer S, Wilson DM, Wolpert H, Wysocki T, Xing D. Continuous glucose monitoring and intensive treatment of type 1 diabetes. N Engl J Med. 2008 Oct 02;359(14):1464–76. doi: 10.1056/NEJMoa0805017.NEJMoa0805017
    1. Hanauer DA, Mei Q, Law J, Khanna R, Zheng K. Supporting information retrieval from electronic health records: a report of University of Michigan's nine-year experience in developing and using the Electronic Medical Record Search Engine (EMERSE) J Biomed Inform. 2015 Jun;55:290–300. doi: 10.1016/j.jbi.2015.05.003. S1532-0464(15)00082-9
    1. Dimidjian S, Barrera M, Martell C, Muñoz RF, Lewinsohn PM. The origins and current status of behavioral activation treatments for depression. Annu Rev Clin Psychol. 2011 Apr 27;7(1):1–38. doi: 10.1146/annurev-clinpsy-032210-104535.
    1. Dimidjian S, Hollon SD, Dobson KS, Schmaling KB, Kohlenberg RJ, Addis ME, Gallop R, McGlinchey JB, Markley DK, Gollan JK, Atkins DC, Dunner DL, Jacobson NS. Randomized trial of behavioral activation, cognitive therapy, and antidepressant medication in the acute treatment of adults with major depression. J Consult Clin Psychol. 2006 Aug;74(4):658–70. doi: 10.1037/0022-006X.74.4.658.2006-09621-003
    1. Jacobson NS, Dobson KS, Truax PA, Addis ME, Koerner K, Gollan JK, Gortner E, Prince SE. A component analysis of cognitive-behavioral treatment for depression. J Consult Clin Psychol. 1996 Apr;64(2):295–304. doi: 10.1037//0022-006x.64.2.295.
    1. Mazzucchelli T, Kane R, Rees C. Behavioral activation treatments for depression in adults: a meta-analysis and review. Clin Psychol Sci Pract. 2009 Dec;16(4):383–411. doi: 10.1111/j.1468-2850.2009.01178.x.
    1. Hart T, Vaccaro M, Collier G, Chervoneva I, Fann JR. Promoting mental health in traumatic brain injury using single-session Behavioural Activation and SMS messaging: a randomized controlled trial. Neuropsychol Rehabil. 2020 Sep 14;30(8):1523–42. doi: 10.1080/09602011.2019.1592761.
    1. Gawrysiak M, Nicholas C, Hopko DR. Behavioral activation for moderately depressed university students: randomized controlled trial. J Counsel Psychol. 2009 Jul;56(3):468–75. doi: 10.1037/a0016383.
    1. Hopko DR, Lejuez CW, Hopko SD. Behavioral activation as an intervention for coexistent depressive and anxiety symptoms. Clin Case Stud. 2016 Jul 21;3(1):37–48. doi: 10.1177/1534650103258969.
    1. Lawton MP, Kleban MH, Moss M, Rovine M, Glicksman A. Measuring caregiving appraisal. J Gerontol. 1989 May 01;44(3):61–71. doi: 10.1093/geronj/44.3.p61.
    1. Struchen MA, Atchison TB, Roebuck TM, Caroselli JS, Sander AM. A multidimensional measure of caregiving appraisal: validation of the Caregiver Appraisal Scale in traumatic brain injury. J Head Trauma Rehabil. 2002 Apr;17(2):132–54. doi: 10.1097/00001199-200204000-00005.
    1. No authors listed Unified Huntington's Disease Rating Scale: reliability and consistency. Huntington Study Group. Mov Disord. 1996 Mar;11(2):136–42. doi: 10.1002/mds.870110204.
    1. Carlozzi NE, Boileau NR, Perlmutter JS, Chou KL, Stout JC, Paulsen JS, McCormack MK, Cella D, Nance MA, Lai J, Dayalu P. Agreement between clinician-rated versus patient-reported outcomes in Huntington disease. J Neurol. 2018 Jun 23;265(6):1443–53. doi: 10.1007/s00415-018-8852-5. 10.1007/s00415-018-8852-5
    1. Boake C. Supervision rating scale: a measure of functional outcome from brain injury. Arch Phys Med Rehabil. 1996 Aug;77(8):765–72. doi: 10.1016/s0003-9993(96)90254-3.
    1. Carlozzi NE, Kallen MA, Hanks R, Hahn EA, Brickell TA, Lange RT, French LM, Kratz AL, Tulsky DS, Cella D, Miner JA, Ianni PA, Sander AM. The TBI-CareQOL Measurement System: development and preliminary validation of health-related quality of life measures for caregivers of civilians and service members/veterans with traumatic brain injury. Arch Phys Med Rehabil. 2019 Apr;100(4S):1–12. doi: 10.1016/j.apmr.2018.08.175. S0003-9993(18)31184-5
    1. Carlozzi NE, Kallen MA, Ianni PA, Hahn EA, French LM, Lange RT, Brickell TA, Hanks R, Sander AM. The development of a new computer-adaptive test to evaluate strain in caregivers of individuals with TBI: TBI-CareQOL Caregiver Strain. Arch Phys Med Rehabil. 2019 Apr;100(4S):13–21. doi: 10.1016/j.apmr.2018.05.033. S0003-9993(18)30395-2
    1. Carlozzi NE, Lange RT, French LM, Sander AM, Ianni PA, Tulsky DS, Miner JA, Kallen MA, Brickell TA. Understanding Health-Related Quality of Life in Caregivers of Civilians and Service Members/Veterans With Traumatic Brain Injury: reliability and validity data for the TBI-CareQOL Measurement System. Arch Phys Med Rehabil. 2019 Apr;100(4S):85–93. doi: 10.1016/j.apmr.2018.05.034. S0003-9993(18)30396-4
    1. Carlozzi NE, Kallen MA, Sander AM, Brickell TA, Lange RT, French LM, Ianni PA, Miner JA, Hanks R. The development of a new computer adaptive test to evaluate anxiety in caregivers of individuals with traumatic brain injury: TBI-CareQOL Caregiver-Specific Anxiety. Arch Phys Med Rehabil. 2019 Apr;100(4S):22–30. doi: 10.1016/j.apmr.2018.05.027. S0003-9993(18)30386-1
    1. Buysse D, Yu L, Moul DE, Germain A, Stover A, Dodds NE, Johnston KL, Shablesky-Cade MA, Pilkonis PA. Development and validation of patient-reported outcome measures for sleep disturbance and sleep-related impairments. Sleep. 2010 Jun;33(6):781–92. doi: 10.1093/sleep/33.6.781.
    1. Cella D, Yount S, Rothrock N, Gershon R, Cook K, Reeve B, Ader D, Fries JF, Bruce B, Rose M, PROMIS Cooperative Group The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years. Med Care. 2007 May;45(5 Suppl 1):3–11. doi: 10.1097/01.mlr.0000258615.42478.55. 00005650-200705001-00002
    1. Bartlett SJ, Orbai A, Duncan T, DeLeon E, Ruffing V, Clegg-Smith K, Bingham CO. Reliability and validity of selected PROMIS measures in people with rheumatoid arthritis. PLoS One. 2015 Sep 17;10(9):e0138543. doi: 10.1371/journal.pone.0138543. PONE-D-15-33217
    1. Quach CW, Langer MM, Chen RC, Thissen D, Usinger DS, Emerson MA, Reeve BB. Reliability and validity of PROMIS measures administered by telephone interview in a longitudinal localized prostate cancer study. Qual Life Res. 2016 Nov 30;25(11):2811–23. doi: 10.1007/s11136-016-1325-3. 10.1007/s11136-016-1325-3
    1. Kappelman MD, Long MD, Martin C, DeWalt DA, Kinneer PM, Chen W, Lewis JD, Sandler RS. Evaluation of the patient-reported outcomes measurement information system in a large cohort of patients with inflammatory bowel diseases. Clin Gastroenterol Hepatol. 2014 Aug;12(8):1315–23. doi: 10.1016/j.cgh.2013.10.019. S1542-3565(13)01673-X
    1. Bajaj J, Thacker LR, Wade JB, Sanyal AJ, Heuman DM, Sterling RK, Gibson DP, Stravitz RT, Puri P, Fuchs M, Luketic V, Noble N, White M, Bell D, Revicki DA. PROMIS computerised adaptive tests are dynamic instruments to measure health-related quality of life in patients with cirrhosis. Aliment Pharmacol Ther. 2011 Nov;34(9):1123–32. doi: 10.1111/j.1365-2036.2011.04842.x. doi: 10.1111/j.1365-2036.2011.04842.x.
    1. Cella David, Riley William, Stone Arthur, Rothrock Nan, Reeve Bryce, Yount Susan, Amtmann Dagmar, Bode Rita, Buysse Daniel, Choi Seung, Cook Karon, Devellis Robert, DeWalt Darren, Fries James F, Gershon Richard, Hahn Elizabeth A, Lai Jin-Shei, Pilkonis Paul, Revicki Dennis, Rose Matthias, Weinfurt Kevin, Hays Ron, PROMIS Cooperative Group The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005-2008. J Clin Epidemiol. 2010 Nov;63(11):1179–94. doi: 10.1016/j.jclinepi.2010.04.011. S0895-4356(10)00173-3
    1. Cook KF, Jensen SE, Schalet BD, Beaumont JL, Amtmann D, Czajkowski S, Dewalt DA, Fries JF, Pilkonis PA, Reeve BB, Stone AA, Weinfurt KP, Cella D. PROMIS measures of pain, fatigue, negative affect, physical function, and social function demonstrated clinical validity across a range of chronic conditions. J Clin Epidemiol. 2016 May;73:89–102. doi: 10.1016/j.jclinepi.2015.08.038. S0895-4356(16)30010-5
    1. Cella D, Lai J, Jensen SE, Christodoulou C, Junghaenel DU, Reeve BB, Stone AA. PROMIS fatigue item bank had clinical validity across diverse chronic conditions. J Clin Epidemiol. 2016 May;73:128–34. doi: 10.1016/j.jclinepi.2015.08.037. S0895-4356(16)00149-9
    1. Kratz AL, Schilling S, Goesling J, Williams DA. The PROMIS FatigueFM Profile: a self-report measure of fatigue for use in fibromyalgia. Qual Life Res. 2016 Jul 28;25(7):1803–13. doi: 10.1007/s11136-016-1230-9. 10.1007/s11136-016-1230-9
    1. Cook KF, Bamer AM, Roddey TS, Kraft GH, Kim J, Amtmann D. A PROMIS fatigue short form for use by individuals who have multiple sclerosis. Qual Life Res. 2012 Aug 17;21(6):1021–30. doi: 10.1007/s11136-011-0011-8.
    1. Tulsky D, Kisala PA, Victorson D, Carlozzi N, Bushnik T, Sherer M, Choi SW, Heinemann AW, Chiaravalloti N, Sander AM, Englander J, Hanks R, Kolakowsky-Hayner S, Roth E, Gershon R, Rosenthal M, Cella DH. TBI-QOL: development and calibration of item banks to measure patient reported outcomes following traumatic brain injury. J Head Trauma Rehabil. 2016;31(1):40–51. doi: 10.1097/HTR.0000000000000131.
    1. Purvis T, Andreou E, Neuman BJ, Riley LH, Skolasky RL. Concurrent validity and responsiveness of PROMIS health domains among patients presenting for anterior cervical spine surgery. Spine (Phila Pa 1976) 2017 Dec 01;42(23):1357–65. doi: 10.1097/BRS.0000000000002347.00007632-201712010-00009
    1. Carlozzi NE, Ianni PA, Tulsky DS, Brickell TA, Lange RT, French LM, Cella D, Kallen MA, Miner JA, Kratz AL. Understanding health-related quality of life in caregivers of civilians and service members/veterans with traumatic brain injury: establishing the reliability and validity of PROMIS fatigue and sleep disturbance item banks. Arch Phys Med Rehabil. 2019 Apr;100(4S):102–9. doi: 10.1016/j.apmr.2018.05.020. S0003-9993(18)30368-X
    1. Carlozzi NE, Hanks R, Lange RT, Brickell TA, Ianni PA, Miner JA, French LM, Kallen MA, Sander AM. Understanding health-related quality of life in caregivers of civilians and service members/veterans with traumatic brain injury: establishing the reliability and validity of PROMIS mental health measures. Arch Phys Med Rehabil. 2019 Apr;100(4S):94–101. doi: 10.1016/j.apmr.2018.05.021. S0003-9993(18)30371-X
    1. Pilkonis PA, Yu L, Dodds NE, Johnston KL, Maihoefer CC, Lawrence SM. Validation of the depression item bank from the Patient-Reported Outcomes Measurement Information System (PROMIS) in a three-month observational study. J Psychiatr Res. 2014 Sep;56:112–9. doi: 10.1016/j.jpsychires.2014.05.010. S0022-3956(14)00148-4
    1. Salsman JM, Butt Z, Pilkonis PA, Cyranowski JM, Zill N, Hendrie HC, Kupst MJ, Kelly MA, Bode RK, Choi SW, Lai J, Griffith JW, Stoney CM, Brouwers P, Knox SS, Cella D. Emotion assessment using the NIH Toolbox. Neurology. 2013 Mar 12;80(11 Suppl 3):S76–86. doi: 10.1212/WNL.0b013e3182872e11. 80/11_Supplement_3/S76
    1. Gruber-Baldini AL, Velozo C, Romero S, Shulman LM. Validation of the PROMIS measures of self-efficacy for managing chronic conditions. Qual Life Res. 2017 Jul 26;26(7):1915–24. doi: 10.1007/s11136-017-1527-3. 10.1007/s11136-017-1527-3
    1. Carlozzi N, Goodnight S, Casaletto KB, Goldsmith A, Heaton RK, Wong AW, Baum CM, Gershon R, Heinemann AW, Tulsky DS. Validation of the NIH Toolbox in individuals with neurologic disorders. Arch Clin Neuropsychol. 2017 Aug 01;32(5):555–73. doi: 10.1093/arclin/acx020. 3074436
    1. Salsman JM, Victorson D, Choi SW, Peterman AH, Heinemann AW, Nowinski C, Cella D. Development and validation of the positive affect and well-being scale for the neurology quality of life (Neuro-QOL) measurement system. Qual Life Res. 2013 Nov 23;22(9):2569–80. doi: 10.1007/s11136-013-0382-0.
    1. Allen J, Alpass FM, Stephens CV. The sensitivity of the MOS SF-12 and PROMIS® global summary scores to adverse health events in an older cohort. Qual Life Res. 2018 Aug 3;27(8):2207–15. doi: 10.1007/s11136-018-1871-y.10.1007/s11136-018-1871-y
    1. Kasturi S, Szymonifka J, Burket JC, Berman JR, Kirou KA, Levine AB, Sammaritano LR, Mandl LA. Feasibility, validity, and reliability of the 10-item patient reported outcomes measurement information system global health short form in outpatients with systemic lupus erythematosus. J Rheumatol. 2018 Mar 01;45(3):397–404. doi: 10.3899/jrheum.170590. jrheum.170590
    1. Katzan IL, Lapin B. PROMIS GH (Patient-Reported Outcomes Measurement Information System Global Health) Scale in Stroke: A Validation Study. Stroke. 2018 Jan;49(1):147–154. doi: 10.1161/STROKEAHA.117.018766.STROKEAHA.117.018766
    1. Lapin B, Thompson NR, Schuster A, Katzan IL. Clinical Utility of Patient-Reported Outcome Measurement Information System Domain Scales. Circ Cardiovasc Qual Outcomes. 2019 Jan;12(1):e004753. doi: 10.1161/CIRCOUTCOMES.118.004753.
    1. Stoop N, Menendez ME, Mellema JJ, Ring D. The PROMIS Global Health Questionnaire correlates with the QuickDASH in patients with upper extremity illness. Hand (N Y) 2018 Jan 13;13(1):118–21. doi: 10.1177/1558944717691127.
    1. Schulz K, Altman D, Moher D, CONSORT Group CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMJ. 2010 Mar 23;340:c332. doi: 10.1136/bmj.c332.
    1. Calvert M, Blazeby J, Altman DG, Revicki DA, Moher D, Brundage MD, CONSORT PRO Group FT. Reporting of patient-reported outcomes in randomized trials: the CONSORT PRO extension. J Am Med Assoc. 2013 Feb 27;309(8):814–22. doi: 10.1001/jama.2013.879.1656259
    1. Schulz K, Altman DG, Moher D, CONSORT Group CONSORT 2010 statement: updated guidelines for reporting parallel group randomized trials. Obstet Gynecol. 2010 May;115(5):1063–70. doi: 10.1097/AOG.0b013e3181d9d421.00006250-201005000-00028
    1. Caregiver statistics: demographics. Caregiver Resource. 2019. [2021-11-04]. .
    1. Reinhard SC, Given B, Petlick NH, Bemis A. Supporting family caregivers in providing care. In: Hughes RG, editor. Patient Safety and Quality: An Evidence-Based Handbook for Nurses. Rockville, MD: Agency for Healthcare Research and Quality and U.S. Department of Health and Human Services; 2008.
    1. Talley RC, Crews JE. Framing the public health of caregiving. Am J Public Health. 2007 Feb;97(2):224–8. doi: 10.2105/AJPH.2004.059337.AJPH.2004.059337

Source: PubMed

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