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Internet and telephone support for discontinuing long-term antidepressants: the REDUCE cluster randomized trial

Internet and telephone support for discontinuing long-term antidepressants: the REDUCE cluster randomized trial
Internet and telephone support for discontinuing long-term antidepressants: the REDUCE cluster randomized trial

Importance: there is significant concern regarding increasing long-term antidepressant treatment for depression beyond an evidence-based duration.

 Objective: to determine whether adding internet and telephone support to a family practitioner review to consider discontinuing long-term antidepressant treatment is safe and more effective than a practitioner review alone. 

Design, Setting, and Participants: in this cluster randomized clinical trial, 131 UK family practices were randomized between December 1, 2018, and March 31, 2022, with remote computerized allocation and 12 months of follow-up. Participants and researchers were aware of allocation, but analysis was blind. Participants were adults who were receiving antidepressants for more than 1 year for a first episode of depression or more than 2 years for recurrent depression who were currently well enough to consider discontinuation and wished to do so and who were at low risk of relapse. Of 6725 patients mailed invitations, 330 (4.9%) were eligible and consented. 

Interventions: internet and telephone self-management support, codesigned and coproduced with patients and practitioners. 

Main Outcomes and Measures: the primary (safety) outcome was depression at 6 months (prespecified complete-case analysis), testing for noninferiority of the intervention to under 2 points on the 9-item Patient Health Questionnaire (PHQ-9). Secondary outcomes (testing for superiority) were antidepressant discontinuation, anxiety, quality of life, antidepressant withdrawal symptoms, mental well-being, enablement, satisfaction, use of health care services, and adverse events. Analyses for the main outcomes were performed on a complete-case basis, and multiple imputation sensitivity analysis was performed on an intention-to-treat basis. 

Results: of 330 participants recruited (325 eligible for inclusion; 178 in intervention practices and 147 in control practices; mean [SD] age at baseline, 54.0 [14.9] years; 223 women [68.6%]), 276 (83.6%) were followed up at 6 months, and 240 (72.7%) at 12 months. The intervention proved noninferior; mean (SD) PHQ-9 scores at 6 months were slightly lower in the intervention arm than in the control arm in the complete-case analysis (4.0 [4.3] vs 5.0 [4.7]; adjusted difference, -1.1; 95% CI, -2.1 to -0.1; P = .03) but not significantly different in an intention-to-treat multiple imputation sensitivity analysis (adjusted difference, -0.9 (95% CI, -1.9 to 0.1; P = .08). By 6 months, antidepressants had been discontinued by 66 of 145 intervention arm participants (45.5%) who provided discontinuation data and 54 of 129 control arm participants (41.9%) (adjusted odds ratio, 1.02; 95% CI, 0.52-1.99; P = .96). In the intervention arm, antidepressant withdrawal symptoms were less severe, and mental well-being was better compared with the control arm; differences were small but significant. There were no significant differences in the other outcomes; 28 of 179 intervention arm participants (15.6%) and 22 of 151 control arm participants (14.6%) experienced adverse events. 

Conclusions and Relevance: in this cluster randomized clinical trial of adding internet and telephone support to a practitioner review for possible antidepressant discontinuation, depression was slightly better with support, but the rate of discontinuation of antidepressants did not significantly increase. Improvements in antidepressant withdrawal symptoms and mental well-being were also small. There were no significant harms. Family practitioner review for possible discontinuation of antidepressants appeared safe and effective for more than 40% of patients willing and well enough to discontinue. Trial Registration: ISRCTN registry Identifiers: ISRCTN15036829 (internal pilot trial) and ISRCTN12417565 (main trial).

Adult, Antidepressive Agents/therapeutic use, Depression/drug therapy, Female, Humans, Internet, Male, Middle Aged, Telephone, United Kingdom
2574-3805
Kendrick, Tony
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Stuart, Beth
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Bowers, Hannah
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Haji Sadeghi, Mahboobeh
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Page, Helen
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Dowrick, Christopher
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Moore, Michael
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Gabbay, Mark
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Leydon, Geraldine M.
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Yao, Guiqing Lily
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Little, Paul
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Griffiths, Gareth
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Lewis, Glyn
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May, Carl
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Moncrieff, Joanna
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Johnson, Chris F.
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Macleod, Una
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Gilbody, Simon
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Dewar-Haggart, Rachel
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Williams, Samantha
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O'Brien, Wendy
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Tiwari, Riya
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Woods, Catherine
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Patel, Tasneem
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Khan, Naila
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van Ginneken, Nadja
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Din, Amy
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Reidy, Claire
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Lucier, Rebecca
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Palmer, Bryan
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Becque, Taeko
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van Leeuwen, Ellen
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Zhu, Shihua
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Geraghty, Adam W.A.
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et al.
Kendrick, Tony
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Stuart, Beth
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Bowers, Hannah
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Haji Sadeghi, Mahboobeh
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Page, Helen
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Dowrick, Christopher
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Moore, Michael
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Gabbay, Mark
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Leydon, Geraldine M.
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Yao, Guiqing Lily
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Little, Paul
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Griffiths, Gareth
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Lewis, Glyn
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May, Carl
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Moncrieff, Joanna
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Johnson, Chris F.
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Macleod, Una
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Gilbody, Simon
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Dewar-Haggart, Rachel
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Williams, Samantha
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O'Brien, Wendy
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Tiwari, Riya
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Woods, Catherine
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Patel, Tasneem
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Khan, Naila
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van Ginneken, Nadja
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Din, Amy
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Reidy, Claire
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Lucier, Rebecca
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Palmer, Bryan
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Becque, Taeko
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van Leeuwen, Ellen
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Zhu, Shihua
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Geraghty, Adam W.A.
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Kendrick, Tony, Stuart, Beth and Bowers, Hannah , et al. (2024) Internet and telephone support for discontinuing long-term antidepressants: the REDUCE cluster randomized trial. JAMA Network Open, 7 (6), [e2418383]. (doi:10.1001/jamanetworkopen.2024.18383).

Record type: Article

Abstract

Importance: there is significant concern regarding increasing long-term antidepressant treatment for depression beyond an evidence-based duration.

 Objective: to determine whether adding internet and telephone support to a family practitioner review to consider discontinuing long-term antidepressant treatment is safe and more effective than a practitioner review alone. 

Design, Setting, and Participants: in this cluster randomized clinical trial, 131 UK family practices were randomized between December 1, 2018, and March 31, 2022, with remote computerized allocation and 12 months of follow-up. Participants and researchers were aware of allocation, but analysis was blind. Participants were adults who were receiving antidepressants for more than 1 year for a first episode of depression or more than 2 years for recurrent depression who were currently well enough to consider discontinuation and wished to do so and who were at low risk of relapse. Of 6725 patients mailed invitations, 330 (4.9%) were eligible and consented. 

Interventions: internet and telephone self-management support, codesigned and coproduced with patients and practitioners. 

Main Outcomes and Measures: the primary (safety) outcome was depression at 6 months (prespecified complete-case analysis), testing for noninferiority of the intervention to under 2 points on the 9-item Patient Health Questionnaire (PHQ-9). Secondary outcomes (testing for superiority) were antidepressant discontinuation, anxiety, quality of life, antidepressant withdrawal symptoms, mental well-being, enablement, satisfaction, use of health care services, and adverse events. Analyses for the main outcomes were performed on a complete-case basis, and multiple imputation sensitivity analysis was performed on an intention-to-treat basis. 

Results: of 330 participants recruited (325 eligible for inclusion; 178 in intervention practices and 147 in control practices; mean [SD] age at baseline, 54.0 [14.9] years; 223 women [68.6%]), 276 (83.6%) were followed up at 6 months, and 240 (72.7%) at 12 months. The intervention proved noninferior; mean (SD) PHQ-9 scores at 6 months were slightly lower in the intervention arm than in the control arm in the complete-case analysis (4.0 [4.3] vs 5.0 [4.7]; adjusted difference, -1.1; 95% CI, -2.1 to -0.1; P = .03) but not significantly different in an intention-to-treat multiple imputation sensitivity analysis (adjusted difference, -0.9 (95% CI, -1.9 to 0.1; P = .08). By 6 months, antidepressants had been discontinued by 66 of 145 intervention arm participants (45.5%) who provided discontinuation data and 54 of 129 control arm participants (41.9%) (adjusted odds ratio, 1.02; 95% CI, 0.52-1.99; P = .96). In the intervention arm, antidepressant withdrawal symptoms were less severe, and mental well-being was better compared with the control arm; differences were small but significant. There were no significant differences in the other outcomes; 28 of 179 intervention arm participants (15.6%) and 22 of 151 control arm participants (14.6%) experienced adverse events. 

Conclusions and Relevance: in this cluster randomized clinical trial of adding internet and telephone support to a practitioner review for possible antidepressant discontinuation, depression was slightly better with support, but the rate of discontinuation of antidepressants did not significantly increase. Improvements in antidepressant withdrawal symptoms and mental well-being were also small. There were no significant harms. Family practitioner review for possible discontinuation of antidepressants appeared safe and effective for more than 40% of patients willing and well enough to discontinue. Trial Registration: ISRCTN registry Identifiers: ISRCTN15036829 (internal pilot trial) and ISRCTN12417565 (main trial).

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Accepted/In Press date: 18 April 2024
Published date: 24 June 2024
Additional Information: Publisher Copyright: © 2024 American Medical Association. All rights reserved.
Keywords: Adult, Antidepressive Agents/therapeutic use, Depression/drug therapy, Female, Humans, Internet, Male, Middle Aged, Telephone, United Kingdom

Identifiers

Local EPrints ID: 491917
URI: http://eprints.soton.ac.uk/id/eprint/491917
ISSN: 2574-3805
PURE UUID: 41dc1ad7-af1d-4fe1-b52e-6836e2100f98
ORCID for Tony Kendrick: ORCID iD orcid.org/0000-0003-1618-9381
ORCID for Hannah Bowers: ORCID iD orcid.org/0000-0002-1996-6652
ORCID for Michael Moore: ORCID iD orcid.org/0000-0002-5127-4509
ORCID for Geraldine M. Leydon: ORCID iD orcid.org/0000-0001-5986-3300
ORCID for Paul Little: ORCID iD orcid.org/0000-0003-3664-1873
ORCID for Gareth Griffiths: ORCID iD orcid.org/0000-0002-9579-8021
ORCID for Carl May: ORCID iD orcid.org/0000-0002-0451-2690
ORCID for Rachel Dewar-Haggart: ORCID iD orcid.org/0000-0002-3757-1152
ORCID for Taeko Becque: ORCID iD orcid.org/0000-0002-0362-3794
ORCID for Adam W.A. Geraghty: ORCID iD orcid.org/0000-0001-7984-8351

Catalogue record

Date deposited: 08 Jul 2024 16:30
Last modified: 11 Dec 2024 02:53

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Contributors

Author: Tony Kendrick ORCID iD
Author: Beth Stuart
Author: Hannah Bowers ORCID iD
Author: Mahboobeh Haji Sadeghi
Author: Helen Page
Author: Christopher Dowrick
Author: Michael Moore ORCID iD
Author: Mark Gabbay
Author: Paul Little ORCID iD
Author: Glyn Lewis
Author: Carl May ORCID iD
Author: Joanna Moncrieff
Author: Chris F. Johnson
Author: Una Macleod
Author: Simon Gilbody
Author: Samantha Williams
Author: Wendy O'Brien
Author: Riya Tiwari
Author: Catherine Woods
Author: Tasneem Patel
Author: Naila Khan
Author: Nadja van Ginneken
Author: Amy Din
Author: Claire Reidy
Author: Rebecca Lucier
Author: Bryan Palmer
Author: Taeko Becque ORCID iD
Author: Ellen van Leeuwen
Author: Shihua Zhu
Corporate Author: et al.

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