Impact of a Mobilized Stress Management Program (Pep-Pal) for Caregivers of Oncology Patients: Mixed-Methods Study

Alaina L Carr, Jacqueline Jones, Susan Mikulich Gilbertson, Mark L Laudenslager, Jean S Kutner, Kristin Kilbourn, Timothy S Sannes, Benjamin W Brewer, Elissa Kolva, Tanisha Joshi, Nicole Amoyal Pensak, Alaina L Carr, Jacqueline Jones, Susan Mikulich Gilbertson, Mark L Laudenslager, Jean S Kutner, Kristin Kilbourn, Timothy S Sannes, Benjamin W Brewer, Elissa Kolva, Tanisha Joshi, Nicole Amoyal Pensak

Abstract

Background: Caregivers of patients with advanced diseases are known to have high levels of distress, including depression and anxiety. Recent research has focused on recognizing caregivers in need of psychosocial support to help them manage their distress. Evidenced-based technological interventions have the potential to aid caregivers in managing distress.

Objective: The objective of our study was to describe caregiver perceptions of the usability and acceptability, and their suggestions for future adaptations, of a mobilized psychoeducation and skills-based intervention.

Methods: This study was a part of a larger trial of a mobilized psychoeducation and skills-based intervention (Psychoeducation and Skills-Based Mobilized Intervention [Pep-Pal]) for caregivers of patients with advanced illness. This substudy used a mixed-methods analysis of quantitative data from all 26 intervention participants and qualitative data from 14 intervention caregivers who completed the Pep-Pal intervention. The qualitative semistructured individual interviews, which we conducted within the first 4 weeks after participants completed the intervention, assessed the acceptability and usability of Pep-Pal. Additionally, the qualitative interviews provided contextual evidence of how the intervention was helpful to interviewees in unanticipated ways. We conducted applied thematic analysis via independent review of transcripts to extract salient themes.

Results: Overall, caregivers of patients with advanced cancer deemed Pep-Pal to be acceptable in all Web-based sessions except for Improving Intimacy. Caregivers perceived the program to be of use across the areas they needed and in others that they had not anticipated. Caregiver recommendations of key changes for the program were to include more variety in caregiver actors in sessions, change the title of Improving Intimacy to Improving Relationships, provide an audio-only option in addition to video, and change the format of the mobilized website program to a stand-alone mobile app.

Conclusions: The valuable feedback in key areas from individual interviews will be integrated into the final version of Pep-Pal that will be tested in a fully powered randomized clinical trial.

Trial registration: ClinicalTrials.gov NCT03002896; https://ichgcp.net/clinical-trials-registry/NCT03002896 (Archived by WebCite at http://www.webcitation.org/76eThwaei).

Keywords: advanced cancer caregivers; bone marrow transplantation; cancer; caregivers; clinical trial, phase I; internet; mHealth; neoplasms; psychoeducation; qualitative research; randomized controlled trial; telemedicine.

Conflict of interest statement

Conflicts of Interest: None declared.

©Alaina L Carr, Jacqueline Jones, Susan Mikulich Gilbertson, Mark L Laudenslager, Jean S Kutner, Kristin Kilbourn, Timothy S Sannes, Benjamin W Brewer, Elissa Kolva, Tanisha Joshi, Nicole Amoyal Pensak. Originally published in JMIR Cancer (http://cancer.jmir.org), 03.05.2019.

Figures

Figure 1
Figure 1
Study flow. BMT: bone marrow transplantation; HADS-A: Hospital Anxiety and Depression Scale subscale for Anxiety.
Figure 2
Figure 2
Mean scores on the Helpfulness of Intervention Sessions Questionnaire by group. A score of 10 indicates a “very helpful” session and 1 indicates a “not at all helpful” session. Error bars are standard deviation.
Figure 3
Figure 3
Mean scores on the Pep-Pal Usability Questionnaire by group. A score of 5 indicates “very strongly agree” and 1 indicates “very strongly disagree”. Error bars are standard deviation.

References

    1. Feinberg L, Reinhard SC, Houser A, Choula R. Valuing the invaluable update - the growing contributions and costs of family caregiving. Washington, DC: AARP Public Policy Institute; 2011. [2018-10-02]. .
    1. Reinhard SC, Feinberg LF, Choula R, Houser A. Valuing the invaluable update: undeniable progress, but big gaps remain. Washington, DC: AARP Public Policy Institute; 2015. Jul, [2018-10-02]. .
    1. The MetLife study of caregiving costs to caregivers. Westport, CT: MetLife Mature Market Institute; 2011. Jun, [2019-03-05]. .
    1. Anderson NB, Bennett Johnson S, Belar CD, Breckler SJ, Nordal KC, Ballard D, Bufka LF. Stress in America: our health at risk. Washington, DC: American Psychological Association; 2012. Jan 11, [2018-10-02]. .
    1. Laudenslager ML, Simoneau TL, Kilbourn K, Natvig C, Philips S, Spradley J, Benitez P, McSweeney P, Mikulich-Gilbertson SK. A randomized control trial of a psychosocial intervention for caregivers of allogeneic hematopoietic stem cell transplant patients: effects on distress. Bone Marrow Transplant. 2015 Aug;50(8):1110–8. doi: 10.1038/bmt.2015.104.
    1. Pensak NA, Joshi T, Simoneau T, Kilbourn K, Carr A, Kutner J, Laudenslager ML. Development of a web-based intervention for addressing distress in caregivers of patients receiving stem cell transplants: formative evaluation with qualitative interviews and focus groups. JMIR Res Protoc. 2017 Dec 22;6(6):e120. doi: 10.2196/resprot.7075.
    1. El-Jawahri AR, Traeger LN, Kuzmuk K, Eusebio JR, Vandusen HB, Shin JA, Keenan T, Gallagher ER, Greer JA, Pirl WF, Jackson VA, Ballen KK, Spitzer TR, Graubert TA, McAfee SL, Dey BR, Chen YA, Temel JS. Quality of life and mood of patients and family caregivers during hospitalization for hematopoietic stem cell transplantation. Cancer. 2015 Mar 15;121(6):951–9. doi: 10.1002/cncr.29149. doi: 10.1002/cncr.29149.
    1. Hudson P, Trauer T, Kelly B, O'Connor M, Thomas K, Zordan R, Summers M. Reducing the psychological distress of family caregivers of home based palliative care patients: longer term effects from a randomised controlled trial. Psychooncology. 2015 Jan;24(1):19–24. doi: 10.1002/pon.3610.
    1. Thygesen KH, Schjødt I, Jarden M. The impact of hematopoietic stem cell transplantation on sexuality: a systematic review of the literature. Bone Marrow Transplant. 2012 May;47(5):716–24. doi: 10.1038/bmt.2011.169.
    1. Watson M, Wheatley K, Harrison GA, Zittoun R, Gray RG, Goldstone AH, Burnett AK. Severe adverse impact on sexual functioning and fertility of bone marrow transplantation, either allogeneic or autologous, compared with consolidation chemotherapy alone: analysis of the MRC AML 10 trial. Cancer. 1999 Oct 1;86(7):1231–9.
    1. Winslow BW. Family caregivers' experiences with community services: a qualitative analysis. Public Health Nurs. 2003 Sep;20(5):341–348. doi: 10.1046/j.1525-1446.2003.20502.x.
    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.
    1. E‑connected family caregiver: bringing caregiving into the 21st century. Bethesda, MD: National Alliance for Caregiving; 2011. Jan, [2018-10-02]. .
    1. DuBenske LL, Gustafson DH, Namkoong K, Hawkins RP, Atwood AK, Brown RL, Chih M, McTavish F, Carmack CL, Buss MK, Govindan R, Cleary JF. CHESS improves cancer caregivers' burden and mood: results of an eHealth RCT. Health Psychol. 2014 Oct;33(10):1261–72. doi: 10.1037/a0034216.
    1. Chi NC, Demiris G. A systematic review of telehealth tools and interventions to support family caregivers. J Telemed Telecare. 2015 Jan;21(1):37–44. doi: 10.1177/1357633X14562734.
    1. What is telehealth? Sacramento, CA: Center for Connected Health Policy, The National Telehealth Policy Resource Center; 2018. [2018-10-02]. .
    1. Ryan P, Lauver DR. The efficacy of tailored interventions. J Nurs Scholarsh. 2002;34(4):331–7.
    1. Northouse LL, Katapodi MC, Song L, Zhang L, Mood DW. Interventions with family caregivers of cancer patients: meta-analysis of randomized trials. CA Cancer J Clin. 2010;60(5):317–39. doi: 10.3322/caac.20081. doi: 10.3322/caac.20081.
    1. Northouse LL, Rosset T, Phillips L, Mood D, Schafenacker A, Kershaw T. Research with families facing cancer: the challenges of accrual and retention. Res Nurs Health. 2006 Jun;29(3):199–211. doi: 10.1002/nur.20128.
    1. Dagan M, Hagedoorn M. Response rates in studies of couples coping with cancer: a systematic review. Health Psychol. 2014 Aug;33(8):845–52. doi: 10.1037/hea0000013.
    1. Kaltenbaugh DJ, Klem ML, Hu L, Turi E, Haines AJ, Hagerty LJ. Using Web-based interventions to support caregivers of patients with cancer: a systematic review. Oncol Nurs Forum. 2015 Mar;42(2):156–64. doi: 10.1188/15.ONF.156-164.
    1. Syrjala KL, Kurland BF, Abrams JR, Sanders JE, Heiman JR. Sexual function changes during the 5 years after high-dose treatment and hematopoietic cell transplantation for malignancy, with case-matched controls at 5 years. Blood. 2008 Feb 1;111(3):989–96. doi: 10.1182/blood-2007-06-096594.
    1. Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta Psychiatr Scand. 1983 Jun;67(6):361–70.
    1. Bjelland I, Dahl AA, Haug TT, Neckelmann D. The validity of the Hospital Anxiety and Depression Scale. An updated literature review. J Psychosom Res. 2002 Feb;52(2):69–77.
    1. Braun V, Clarke V. Using thematic analysis in psychology. Qual Res Psychol. 2006 Jan;3(2):77–101. doi: 10.1191/1478088706qp063oa.
    1. Creswell JW, Poth CN. Qualitative Inquiry and Research Design: Choosing among Five Approaches. Thousand Oaks, CA: SAGE Publications, Inc; 2018.
    1. Nielsen MK, Neergaard MA, Jensen AB, Bro F, Guldin M. Do we need to change our understanding of anticipatory grief in caregivers? A systematic review of caregiver studies during end-of-life caregiving and bereavement. Clin Psychol Rev. 2016 Mar;44:75–93. doi: 10.1016/j.cpr.2016.01.002.
    1. Gallagher-Thompson D, Coon DW. Evidence-based psychological treatments for distress in family caregivers of older adults. Psychol Aging. 2007 Mar;22(1):37–51. doi: 10.1037/0882-7974.22.1.37.
    1. Northouse L, Williams A, Given B, McCorkle R. Psychosocial care for family caregivers of patients with cancer. J Clin Oncol. 2012 Apr 10;30(11):1227–34. doi: 10.1200/JCO.2011.39.5798.
    1. Posluszny DM, Dougall AL, Johnson JT, Argiris A, Ferris RL, Baum A, Bovbjerg DH, Dew MA. Posttraumatic stress disorder symptoms in newly diagnosed patients with head and neck cancer and their partners. Head Neck. 2015 Sep;37(9):1282–9. doi: 10.1002/hed.23760.

Source: PubMed

Подписаться