Development and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients.

dc.contributor.authorLichtenthal, W. G.
dc.contributor.authorViola, M.
dc.contributor.authorRogers, M.
dc.contributor.authorRoberts, Kailey E.
dc.contributor.authorLief, L.
dc.contributor.authorCox, C. E.
dc.contributor.authorBrewin, C. R.
dc.contributor.authorXu, J. C.
dc.contributor.authorMaciejewski, P. K.
dc.contributor.authorPan, C. X.
dc.contributor.authorCoats, T.
dc.contributor.authorOuyang, D. J.
dc.contributor.authorRabin, S.
dc.contributor.authorVaughan, S. C.
dc.contributor.authorBreibart, W.
dc.contributor.authorMarenberg, M. E.
dc.contributor.authorPrigerson, H. G.
dc.date.accessioned2023-10-27T14:34:11Z
dc.date.available2023-10-27T14:34:11Z
dc.date.issued2021
dc.descriptionScholarly articleen_US
dc.description.abstract_Abstract_ _Objective._ The objectives of this study were to develop and refine EMPOWER (Enhancing and Mobilizing the POtential for Wellness and Resilience), a brief manualized cognitivebehavioral, acceptance-based intervention for surrogate decision-makers of critically ill patients and to evaluate its preliminary feasibility, acceptability, and promise in improving surrogates’ mental health and patient outcomes. _Method._ Part 1 involved obtaining qualitative stakeholder feedback from 5 bereaved surrogates and 10 critical care and mental health clinicians. Stakeholders were provided with the manual and prompted for feedback on its content, format, and language. Feedback was organized and incorporated into the manual, which was then re-circulated until consensus. In Part 2, surrogates of critically ill patients admitted to an intensive care unit (ICU) reporting moderate anxiety or close attachment were enrolled in an open trial of EMPOWER. Surrogates completed six, 15–20 min modules, totaling 1.5–2 h. Surrogates were administered measures of peritraumatic distress, experiential avoidance, prolonged grief, distress tolerance, anxiety, and depression at pre-intervention, post-intervention, and at 1-month and 3-month follow-up assessments. Results. Part 1 resulted in changes to the EMPOWER manual, including reducing jargon, improving navigability, making EMPOWER applicable for a range of illness scenarios, rearranging the modules, and adding further instructions and psychoeducation. Part 2 findings suggested that EMPOWER is feasible, with 100% of participants completing all modules. The acceptability of EMPOWER appeared strong, with high ratings of effectiveness and helpfulness (M= 8/10). _Results_ showed immediate post-intervention improvements in anxiety (d = −0.41), peritraumatic distress (d = −0.24), and experiential avoidance (d = −0.23). At the 3-month follow-up assessments, surrogates exhibited improvements in prolonged grief symptoms (d = −0.94), depression (d = −0.23), anxiety (d = −0.29), and experiential avoidance (d = −0.30). _Significance of results._ Preliminary data suggest that EMPOWER is feasible, acceptable, and associated with notable improvements in psychological symptoms among surrogates. Future research should examine EMPOWER with a larger sample in a randomized controlled trial.en_US
dc.description.sponsorship_Funding_ This research was supported by National Cancer Institute (NCI) grant R21CA218313 (Prigerson/Lichtenthal) and American Cancer Society grant 130534-PEP-17-053-01-PCSM. Research efforts were additionally supported by NCI grants R35CA197730 (Prigerson), K07CA172216 (Lichtenthal), P30CA008748 (Thompson), and T32CA009461 (Ostroff).en_US
dc.identifier.citationLichtenthal, W. G., Viola, M., Rogers, M., Roberts, K. E., Lief, L., Cox, C. E., Brewin, C. R., Xu, J. C., Maciejewski, P. K., Pan, C. X., Coats, T., Ouyang, D. J., Rabin, S., Vaughan, S. C., Breitbart, W., Marenberg, M. E., & Prigerson, H. G. (2021). Development and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients. Palliative & Supportive Care, 20, 1–11. https://doi.org/10.1017/S1478951521000626en_US
dc.identifier.doihttps://doi.org/10.1017/S1478951521000626en_US
dc.identifier.issn1478-9515, 1478-9523
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741895/en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12202/9386
dc.language.isoen_USen_US
dc.publisherCambridge UPen_US
dc.relation.ispartofseriesPalliative & Supportive Care;
dc.relation.ispartofseries;20
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectCritical careen_US
dc.subjectGriefen_US
dc.subjectIntensive care uniten_US
dc.subjectInterventionen_US
dc.subjectSurrogate decision-makingen_US
dc.titleDevelopment and preliminary evaluation of EMPOWER for surrogate decision-makers of critically ill patients.en_US
dc.typeArticleen_US
local.yu.facultypagehttps://www.yu.edu/faculty/pages/roberts-kaileyen_US

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