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A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol
BACKGROUND: Depressed patients commonly experience psychological pain. Research pointed to positive psychological interventions as an effective means of ameliorating psychological pain, although the exact effect is unclear. Based on the hope theory and solution-focused brief therapy (SFBT), this stu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084640/ https://www.ncbi.nlm.nih.gov/pubmed/37038115 http://dx.doi.org/10.1186/s12912-023-01252-6 |
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author | Chen, Shu-Yan Bian, Cheng Cheng, Yin Zhao, Wei-Wei Yan, Shi-Rui Zhang, Yan-Hong |
author_facet | Chen, Shu-Yan Bian, Cheng Cheng, Yin Zhao, Wei-Wei Yan, Shi-Rui Zhang, Yan-Hong |
author_sort | Chen, Shu-Yan |
collection | PubMed |
description | BACKGROUND: Depressed patients commonly experience psychological pain. Research pointed to positive psychological interventions as an effective means of ameliorating psychological pain, although the exact effect is unclear. Based on the hope theory and solution-focused brief therapy (SFBT), this study combines hope theory with solution-focused brief therapy to develop a nurse-led psychological pain solution-focused (PPSF) intervention in depressed patients. METHODS: This is an assessor-blinded randomized controlled trial following the SPIRIT guidance. A total of 84 depressed patients will be recruited from the inpatient wards of a psychiatric hospital and randomly assigned to the control and experimental groups. Patients in the control group will be treated as usual. In contrast, patients in the experimental group will receive 6 sessions of the PPSF intervention for two weeks on top of the routine care. Primary outcomes are psychological pain, hope, cognitive distortions. Secondary outcomes are depression and suicidal ideation. Data will be collected at 5-time points: baseline, 1 and 2 weeks (post-intervention), 1 month (follow up), and 6 months after baseline. Generalized equation evaluation will be used to assess the effectiveness of the PPSF intervention. DISCUSSION: From a positive psychology perspective, there remains much room for developing psychological pain interventions in depressed patients. SFBT and hope theory are both based on positive psychology. With hope theory as the general framework and SFBT questions as the practical guide, the PPSF intervention program is designed that nursing staff can implement. If the intervention is effective, it will advance the development of psychological pain interventions for patients with depression. TRIAL REGISTRATION: ChiCTR2100048223 |
format | Online Article Text |
id | pubmed-10084640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100846402023-04-11 A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol Chen, Shu-Yan Bian, Cheng Cheng, Yin Zhao, Wei-Wei Yan, Shi-Rui Zhang, Yan-Hong BMC Nurs Study Protocol BACKGROUND: Depressed patients commonly experience psychological pain. Research pointed to positive psychological interventions as an effective means of ameliorating psychological pain, although the exact effect is unclear. Based on the hope theory and solution-focused brief therapy (SFBT), this study combines hope theory with solution-focused brief therapy to develop a nurse-led psychological pain solution-focused (PPSF) intervention in depressed patients. METHODS: This is an assessor-blinded randomized controlled trial following the SPIRIT guidance. A total of 84 depressed patients will be recruited from the inpatient wards of a psychiatric hospital and randomly assigned to the control and experimental groups. Patients in the control group will be treated as usual. In contrast, patients in the experimental group will receive 6 sessions of the PPSF intervention for two weeks on top of the routine care. Primary outcomes are psychological pain, hope, cognitive distortions. Secondary outcomes are depression and suicidal ideation. Data will be collected at 5-time points: baseline, 1 and 2 weeks (post-intervention), 1 month (follow up), and 6 months after baseline. Generalized equation evaluation will be used to assess the effectiveness of the PPSF intervention. DISCUSSION: From a positive psychology perspective, there remains much room for developing psychological pain interventions in depressed patients. SFBT and hope theory are both based on positive psychology. With hope theory as the general framework and SFBT questions as the practical guide, the PPSF intervention program is designed that nursing staff can implement. If the intervention is effective, it will advance the development of psychological pain interventions for patients with depression. TRIAL REGISTRATION: ChiCTR2100048223 BioMed Central 2023-04-10 /pmc/articles/PMC10084640/ /pubmed/37038115 http://dx.doi.org/10.1186/s12912-023-01252-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Study Protocol Chen, Shu-Yan Bian, Cheng Cheng, Yin Zhao, Wei-Wei Yan, Shi-Rui Zhang, Yan-Hong A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title | A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title_full | A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title_fullStr | A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title_full_unstemmed | A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title_short | A randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
title_sort | randomized controlled trial of a nurse-led psychological pain solution-focused intervention for depressed inpatients: study protocol |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084640/ https://www.ncbi.nlm.nih.gov/pubmed/37038115 http://dx.doi.org/10.1186/s12912-023-01252-6 |
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