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Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study
PURPOSE: The purpose of the present study was to conduct a preliminary evaluation of the feasibility and impact of a risk-targeted behavioral activation intervention for work-disabled individuals with comorbid pain and depression. METHODS: The design of the study was a single-arm non-randomized tria...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034524/ https://www.ncbi.nlm.nih.gov/pubmed/35461255 http://dx.doi.org/10.1186/s40814-022-01040-0 |
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author | Sullivan, Michael J. L. Wideman, Timothy H. Gauthier, Nathalie Thibault, Pascal Ellis, Tamra Adams, Heather |
author_facet | Sullivan, Michael J. L. Wideman, Timothy H. Gauthier, Nathalie Thibault, Pascal Ellis, Tamra Adams, Heather |
author_sort | Sullivan, Michael J. L. |
collection | PubMed |
description | PURPOSE: The purpose of the present study was to conduct a preliminary evaluation of the feasibility and impact of a risk-targeted behavioral activation intervention for work-disabled individuals with comorbid pain and depression. METHODS: The design of the study was a single-arm non-randomized trial. The sample consisted of 66 work-disabled individuals with comorbid pain and depression. The treatment program consisted of a 10-week standardized behavioral activation intervention supplemented by techniques to target two psychosocial risk factors for delayed recovery, namely, catastrophic thinking and perceptions of injustice. Measures of pain severity, depression, catastrophic thinking, perceived injustice, and self-reported disability were completed pre-, mid-, and post-treatment. Satisfaction with treatment was assessed at post-treatment. Return to work was assessed at 6-month follow-up. RESULTS: The drop-out rate was 18%. At treatment termination, 91% of participants indicated that they were “very” or “completely” satisfied with their involvement in the treatment program. Significant reductions in pain (Cohen’s d = 0.71), depression (d = 0.86), catastrophic thinking (d = 1.1), and perceived injustice (d = 1.0) were observed through the course of treatment. In multivariate analyses, treatment-related reductions in depression, catastrophic thinking, and perceived injustice, but not pain, contributed significant unique variance to the prediction of return-to-work outcomes. CONCLUSIONS: Risk-targeted behavioral activation was found to be an acceptable and effective intervention for work-disabled individuals with comorbid pain and depression. The findings suggest that interventions targeting psychosocial risk factors for pain and depression might contribute to more positive recovery outcomes in work-disabled individuals with comorbid pain and depression. TRIAL REGISTRATION: ClinicalTrials.gov: NCT0517442. Retrospectively registered. |
format | Online Article Text |
id | pubmed-9034524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90345242022-04-24 Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study Sullivan, Michael J. L. Wideman, Timothy H. Gauthier, Nathalie Thibault, Pascal Ellis, Tamra Adams, Heather Pilot Feasibility Stud Research PURPOSE: The purpose of the present study was to conduct a preliminary evaluation of the feasibility and impact of a risk-targeted behavioral activation intervention for work-disabled individuals with comorbid pain and depression. METHODS: The design of the study was a single-arm non-randomized trial. The sample consisted of 66 work-disabled individuals with comorbid pain and depression. The treatment program consisted of a 10-week standardized behavioral activation intervention supplemented by techniques to target two psychosocial risk factors for delayed recovery, namely, catastrophic thinking and perceptions of injustice. Measures of pain severity, depression, catastrophic thinking, perceived injustice, and self-reported disability were completed pre-, mid-, and post-treatment. Satisfaction with treatment was assessed at post-treatment. Return to work was assessed at 6-month follow-up. RESULTS: The drop-out rate was 18%. At treatment termination, 91% of participants indicated that they were “very” or “completely” satisfied with their involvement in the treatment program. Significant reductions in pain (Cohen’s d = 0.71), depression (d = 0.86), catastrophic thinking (d = 1.1), and perceived injustice (d = 1.0) were observed through the course of treatment. In multivariate analyses, treatment-related reductions in depression, catastrophic thinking, and perceived injustice, but not pain, contributed significant unique variance to the prediction of return-to-work outcomes. CONCLUSIONS: Risk-targeted behavioral activation was found to be an acceptable and effective intervention for work-disabled individuals with comorbid pain and depression. The findings suggest that interventions targeting psychosocial risk factors for pain and depression might contribute to more positive recovery outcomes in work-disabled individuals with comorbid pain and depression. TRIAL REGISTRATION: ClinicalTrials.gov: NCT0517442. Retrospectively registered. BioMed Central 2022-04-23 /pmc/articles/PMC9034524/ /pubmed/35461255 http://dx.doi.org/10.1186/s40814-022-01040-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sullivan, Michael J. L. Wideman, Timothy H. Gauthier, Nathalie Thibault, Pascal Ellis, Tamra Adams, Heather Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title | Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title_full | Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title_fullStr | Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title_full_unstemmed | Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title_short | Risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
title_sort | risk-targeted behavioral activation for the management of work disability associated with comorbid pain and depression: a feasibility study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034524/ https://www.ncbi.nlm.nih.gov/pubmed/35461255 http://dx.doi.org/10.1186/s40814-022-01040-0 |
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