Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer: The REBECCA Randomized Clinical Trial

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer : The REBECCA Randomized Clinical Trial. / Bidstrup, Pernille Envold; Johansen, Christoffer; Kroman, Niels; Belmonte, Federica; Duriaud, Helle; Dalton, Susanne Oksbjerg; Andersen, Kenneth Geving; Mertz, Birgitte.

In: JAMA network open, Vol. 6, No. 6, e2319591, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bidstrup, PE, Johansen, C, Kroman, N, Belmonte, F, Duriaud, H, Dalton, SO, Andersen, KG & Mertz, B 2023, 'Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer: The REBECCA Randomized Clinical Trial', JAMA network open, vol. 6, no. 6, e2319591. https://doi.org/10.1001/jamanetworkopen.2023.19591

APA

Bidstrup, P. E., Johansen, C., Kroman, N., Belmonte, F., Duriaud, H., Dalton, S. O., Andersen, K. G., & Mertz, B. (2023). Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer: The REBECCA Randomized Clinical Trial. JAMA network open, 6(6), [e2319591]. https://doi.org/10.1001/jamanetworkopen.2023.19591

Vancouver

Bidstrup PE, Johansen C, Kroman N, Belmonte F, Duriaud H, Dalton SO et al. Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer: The REBECCA Randomized Clinical Trial. JAMA network open. 2023;6(6). e2319591. https://doi.org/10.1001/jamanetworkopen.2023.19591

Author

Bidstrup, Pernille Envold ; Johansen, Christoffer ; Kroman, Niels ; Belmonte, Federica ; Duriaud, Helle ; Dalton, Susanne Oksbjerg ; Andersen, Kenneth Geving ; Mertz, Birgitte. / Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer : The REBECCA Randomized Clinical Trial. In: JAMA network open. 2023 ; Vol. 6, No. 6.

Bibtex

@article{fe810158834b45ecbca3a6aeaf4762db,
title = "Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer: The REBECCA Randomized Clinical Trial",
abstract = "Importance: The unmet needs regarding symptom management of psychological distress among patients with breast cancer must be addressed. However, little evidence exists on effective interventions, such as nurse navigation. Objective: To compare the long-term effects of the REBECCA (Rehabilitation After Breast Cancer) nurse navigation intervention vs usual care in patients with breast cancer who were psychologically vulnerable. Design, Setting, and Participants: This parallel randomized clinical trial recruited and evaluated for eligibility adult female patients with newly diagnosed breast cancer and symptoms of psychological distress (distress score of ≥7 points on Distress Thermometer) at Rigshospitalet in Copenhagen, Denmark, from August 2017 to October 2019. This study continued the work of a pilot study, extending the follow-up to 18 months. Patients who met the inclusion criteria were randomized to either standard care or the REBECCA intervention. Intention-to-treat analyses were performed from June 2021 to October 2022. Interventions: Patients who were randomized to the REBECCA intervention received nurse navigation and symptom screening as well as standard care. Standard care included regular treatment, nurse support at chemotherapy and radiotherapy appointments, and municipality-based rehabilitation. Main Outcomes and Measures: The primary outcome was distress, as measured using the Distress Thermometer. The secondary outcomes included symptoms of anxiety, symptoms of depression, breast cancer-specific health-related quality of life, fear of recurrence, sleep, cognitive function, patient activation, pain, health behavior, body mass index, and need for support. Long-term effects at 6, 12, and 18 months were examined using mixed-effect models, adjusting for randomization strata of age and treatment modality. Results: A total of 309 female patients were included in the analysis, with 153 patients randomized to the standard care group and 156 patients randomized to the REBECCA intervention group. Mean (SD) age was 56 (11) years with only small between-group differences. Patients receiving the REBECCA intervention compared with standard care had reduced (although not significant) symptoms of distress, especially at the 12-month follow-up (estimated effect = -0.51 [95% CI, -1.05 to 0.04]; effect size [ES] = -0.49). Significant effects were seen for symptoms of depression at 6 months (estimated effect = -1.39 [95% CI, -2.33 to -0.44]; ES = -0.27), and breast cancer-specific health-related quality of life at 12 months (estimated effect = 4.03 [95% CI, 1.28- 6.77]; ES = 0.31). Nonsignificant reductions were seen for symptoms of anxiety at 6 months (estimated effect = -1.00 [95% CI, -1.95 to -0.06]; ES = -0.21) and 12 months (estimated effect = -1.01 [95% CI, -1.97 to -0.04]; ES = -0.21), and a nonsignificant increase was seen for patient activation at 18 months (estimated effect = 3.52 [95% CI, -0.09 to 7.12]; ES = 0.25). Stronger intervention effects were observed for younger age, low patient activation, less education, and low social support. Conclusions and Relevance: Results of this study indicate that patients with breast cancer who were psychologically vulnerable (ie, having moderate to high psychological distress) did not experience significant reduction in distress with nurse navigation. Further research is needed to develop the intervention's framework and investigate its potential use in clinical practice. Trial Registration: ClinicalTrials.gov Identifier: NCT03254875.",
author = "Bidstrup, {Pernille Envold} and Christoffer Johansen and Niels Kroman and Federica Belmonte and Helle Duriaud and Dalton, {Susanne Oksbjerg} and Andersen, {Kenneth Geving} and Birgitte Mertz",
note = "Publisher Copyright: {\textcopyright} 2023 American Medical Association. All rights reserved.",
year = "2023",
doi = "10.1001/jamanetworkopen.2023.19591",
language = "English",
volume = "6",
journal = "JAMA network open",
issn = "2574-3805",
publisher = "American Medical Association",
number = "6",

}

RIS

TY - JOUR

T1 - Effect of a Nurse Navigation Intervention on Mental Symptoms in Patients with Psychological Vulnerability and Breast Cancer

T2 - The REBECCA Randomized Clinical Trial

AU - Bidstrup, Pernille Envold

AU - Johansen, Christoffer

AU - Kroman, Niels

AU - Belmonte, Federica

AU - Duriaud, Helle

AU - Dalton, Susanne Oksbjerg

AU - Andersen, Kenneth Geving

AU - Mertz, Birgitte

N1 - Publisher Copyright: © 2023 American Medical Association. All rights reserved.

PY - 2023

Y1 - 2023

N2 - Importance: The unmet needs regarding symptom management of psychological distress among patients with breast cancer must be addressed. However, little evidence exists on effective interventions, such as nurse navigation. Objective: To compare the long-term effects of the REBECCA (Rehabilitation After Breast Cancer) nurse navigation intervention vs usual care in patients with breast cancer who were psychologically vulnerable. Design, Setting, and Participants: This parallel randomized clinical trial recruited and evaluated for eligibility adult female patients with newly diagnosed breast cancer and symptoms of psychological distress (distress score of ≥7 points on Distress Thermometer) at Rigshospitalet in Copenhagen, Denmark, from August 2017 to October 2019. This study continued the work of a pilot study, extending the follow-up to 18 months. Patients who met the inclusion criteria were randomized to either standard care or the REBECCA intervention. Intention-to-treat analyses were performed from June 2021 to October 2022. Interventions: Patients who were randomized to the REBECCA intervention received nurse navigation and symptom screening as well as standard care. Standard care included regular treatment, nurse support at chemotherapy and radiotherapy appointments, and municipality-based rehabilitation. Main Outcomes and Measures: The primary outcome was distress, as measured using the Distress Thermometer. The secondary outcomes included symptoms of anxiety, symptoms of depression, breast cancer-specific health-related quality of life, fear of recurrence, sleep, cognitive function, patient activation, pain, health behavior, body mass index, and need for support. Long-term effects at 6, 12, and 18 months were examined using mixed-effect models, adjusting for randomization strata of age and treatment modality. Results: A total of 309 female patients were included in the analysis, with 153 patients randomized to the standard care group and 156 patients randomized to the REBECCA intervention group. Mean (SD) age was 56 (11) years with only small between-group differences. Patients receiving the REBECCA intervention compared with standard care had reduced (although not significant) symptoms of distress, especially at the 12-month follow-up (estimated effect = -0.51 [95% CI, -1.05 to 0.04]; effect size [ES] = -0.49). Significant effects were seen for symptoms of depression at 6 months (estimated effect = -1.39 [95% CI, -2.33 to -0.44]; ES = -0.27), and breast cancer-specific health-related quality of life at 12 months (estimated effect = 4.03 [95% CI, 1.28- 6.77]; ES = 0.31). Nonsignificant reductions were seen for symptoms of anxiety at 6 months (estimated effect = -1.00 [95% CI, -1.95 to -0.06]; ES = -0.21) and 12 months (estimated effect = -1.01 [95% CI, -1.97 to -0.04]; ES = -0.21), and a nonsignificant increase was seen for patient activation at 18 months (estimated effect = 3.52 [95% CI, -0.09 to 7.12]; ES = 0.25). Stronger intervention effects were observed for younger age, low patient activation, less education, and low social support. Conclusions and Relevance: Results of this study indicate that patients with breast cancer who were psychologically vulnerable (ie, having moderate to high psychological distress) did not experience significant reduction in distress with nurse navigation. Further research is needed to develop the intervention's framework and investigate its potential use in clinical practice. Trial Registration: ClinicalTrials.gov Identifier: NCT03254875.

AB - Importance: The unmet needs regarding symptom management of psychological distress among patients with breast cancer must be addressed. However, little evidence exists on effective interventions, such as nurse navigation. Objective: To compare the long-term effects of the REBECCA (Rehabilitation After Breast Cancer) nurse navigation intervention vs usual care in patients with breast cancer who were psychologically vulnerable. Design, Setting, and Participants: This parallel randomized clinical trial recruited and evaluated for eligibility adult female patients with newly diagnosed breast cancer and symptoms of psychological distress (distress score of ≥7 points on Distress Thermometer) at Rigshospitalet in Copenhagen, Denmark, from August 2017 to October 2019. This study continued the work of a pilot study, extending the follow-up to 18 months. Patients who met the inclusion criteria were randomized to either standard care or the REBECCA intervention. Intention-to-treat analyses were performed from June 2021 to October 2022. Interventions: Patients who were randomized to the REBECCA intervention received nurse navigation and symptom screening as well as standard care. Standard care included regular treatment, nurse support at chemotherapy and radiotherapy appointments, and municipality-based rehabilitation. Main Outcomes and Measures: The primary outcome was distress, as measured using the Distress Thermometer. The secondary outcomes included symptoms of anxiety, symptoms of depression, breast cancer-specific health-related quality of life, fear of recurrence, sleep, cognitive function, patient activation, pain, health behavior, body mass index, and need for support. Long-term effects at 6, 12, and 18 months were examined using mixed-effect models, adjusting for randomization strata of age and treatment modality. Results: A total of 309 female patients were included in the analysis, with 153 patients randomized to the standard care group and 156 patients randomized to the REBECCA intervention group. Mean (SD) age was 56 (11) years with only small between-group differences. Patients receiving the REBECCA intervention compared with standard care had reduced (although not significant) symptoms of distress, especially at the 12-month follow-up (estimated effect = -0.51 [95% CI, -1.05 to 0.04]; effect size [ES] = -0.49). Significant effects were seen for symptoms of depression at 6 months (estimated effect = -1.39 [95% CI, -2.33 to -0.44]; ES = -0.27), and breast cancer-specific health-related quality of life at 12 months (estimated effect = 4.03 [95% CI, 1.28- 6.77]; ES = 0.31). Nonsignificant reductions were seen for symptoms of anxiety at 6 months (estimated effect = -1.00 [95% CI, -1.95 to -0.06]; ES = -0.21) and 12 months (estimated effect = -1.01 [95% CI, -1.97 to -0.04]; ES = -0.21), and a nonsignificant increase was seen for patient activation at 18 months (estimated effect = 3.52 [95% CI, -0.09 to 7.12]; ES = 0.25). Stronger intervention effects were observed for younger age, low patient activation, less education, and low social support. Conclusions and Relevance: Results of this study indicate that patients with breast cancer who were psychologically vulnerable (ie, having moderate to high psychological distress) did not experience significant reduction in distress with nurse navigation. Further research is needed to develop the intervention's framework and investigate its potential use in clinical practice. Trial Registration: ClinicalTrials.gov Identifier: NCT03254875.

UR - http://www.scopus.com/inward/record.url?scp=85162753894&partnerID=8YFLogxK

U2 - 10.1001/jamanetworkopen.2023.19591

DO - 10.1001/jamanetworkopen.2023.19591

M3 - Journal article

C2 - 37351885

AN - SCOPUS:85162753894

VL - 6

JO - JAMA network open

JF - JAMA network open

SN - 2574-3805

IS - 6

M1 - e2319591

ER -

ID: 370212854