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Article: High-definition transcranial direct current stimulation (HD-tDCS) as augmentation therapy in late-life depression (LLD) with suboptimal response to treatment-a study protocol for a double-blinded randomized sham-controlled trial

TitleHigh-definition transcranial direct current stimulation (HD-tDCS) as augmentation therapy in late-life depression (LLD) with suboptimal response to treatment-a study protocol for a double-blinded randomized sham-controlled trial
Authors
KeywordsAugmentation therapy
High-definition transcranial direct current stimulation
Late-life depression
Issue Date28-Oct-2022
PublisherBioMed Central
Citation
Trials, 2022, v. 23, n. 1 How to Cite?
AbstractBackground: Late-life depression (LLD) has a poorer prognosis and higher relapse rate than younger adults, with up to one third of patients with LLD showing suboptimal response to antidepressant therapy. LLD has been associated with significant impairment in cognition and daily functioning. Few studies have evaluated the therapeutic effects of high-definition transcranial direct current stimulation (HD-tDCS) on depressive and cognitive symptoms of LLD. The current randomized controlled trial assesses the efficacy of HD-tDCS as an augmentation therapy with antidepressants compared to sham-control in subjects with LLD.Methods: Fifty-eight patients with LLD will be recruited and randomly assigned to the active HD-tDCS or sham HD-tDCS group. In both groups, patients will receive the active or sham intervention in addition to their pre-existing antidepressant therapy, for 2 weeks with 5 sessions per week, each lasting 30 min. The primary outcome measures will be the change of depressive symptoms, clinical response and the remission rate as measured with the Hamilton Depression Rating scale (HAMD-17) before and after the intervention, and at the 4th and 12th week after the completed intervention. Secondary outcome measures include cognitive symptoms, anxiety symptoms, daily functioning and adverse effects.Discussion: Older adults with depression are associated with poorer outcomes or unsatisfactory responses to antidepressant therapy, and significant cognitive decline. Therefore, a new effective treatment option is needed. This randomized control trial aims at assessing the efficacy of HD-tDCS on ameliorating the depressive, cognitive and anxiety symptoms, and improving the daily functioning of subjects with LLD.
Persistent Identifierhttp://hdl.handle.net/10722/342153
ISSN
2021 Impact Factor: 2.728
2020 SCImago Journal Rankings: 1.067
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorNgan, STJ-
dc.contributor.authorChan, LK-
dc.contributor.authorChan, WC-
dc.contributor.authorLam, LCW-
dc.contributor.authorLi, WK-
dc.contributor.authorLim, K-
dc.contributor.authorOr, E-
dc.contributor.authorPang, PF-
dc.contributor.authorPoon, TK-
dc.contributor.authorWong, MCM-
dc.contributor.authorWu, YKA-
dc.contributor.authorCheng, PWC-
dc.date.accessioned2024-04-17T03:49:38Z-
dc.date.available2024-04-17T03:49:38Z-
dc.date.issued2022-10-28-
dc.identifier.citationTrials, 2022, v. 23, n. 1-
dc.identifier.issn1745-6215-
dc.identifier.urihttp://hdl.handle.net/10722/342153-
dc.description.abstractBackground: Late-life depression (LLD) has a poorer prognosis and higher relapse rate than younger adults, with up to one third of patients with LLD showing suboptimal response to antidepressant therapy. LLD has been associated with significant impairment in cognition and daily functioning. Few studies have evaluated the therapeutic effects of high-definition transcranial direct current stimulation (HD-tDCS) on depressive and cognitive symptoms of LLD. The current randomized controlled trial assesses the efficacy of HD-tDCS as an augmentation therapy with antidepressants compared to sham-control in subjects with LLD.Methods: Fifty-eight patients with LLD will be recruited and randomly assigned to the active HD-tDCS or sham HD-tDCS group. In both groups, patients will receive the active or sham intervention in addition to their pre-existing antidepressant therapy, for 2 weeks with 5 sessions per week, each lasting 30 min. The primary outcome measures will be the change of depressive symptoms, clinical response and the remission rate as measured with the Hamilton Depression Rating scale (HAMD-17) before and after the intervention, and at the 4th and 12th week after the completed intervention. Secondary outcome measures include cognitive symptoms, anxiety symptoms, daily functioning and adverse effects.Discussion: Older adults with depression are associated with poorer outcomes or unsatisfactory responses to antidepressant therapy, and significant cognitive decline. Therefore, a new effective treatment option is needed. This randomized control trial aims at assessing the efficacy of HD-tDCS on ameliorating the depressive, cognitive and anxiety symptoms, and improving the daily functioning of subjects with LLD.-
dc.languageeng-
dc.publisherBioMed Central-
dc.relation.ispartofTrials-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAugmentation therapy-
dc.subjectHigh-definition transcranial direct current stimulation-
dc.subjectLate-life depression-
dc.titleHigh-definition transcranial direct current stimulation (HD-tDCS) as augmentation therapy in late-life depression (LLD) with suboptimal response to treatment-a study protocol for a double-blinded randomized sham-controlled trial-
dc.typeArticle-
dc.identifier.doi10.1186/s13063-022-06855-z-
dc.identifier.pmid36307858-
dc.identifier.scopuseid_2-s2.0-85140918543-
dc.identifier.volume23-
dc.identifier.issue1-
dc.identifier.eissn1745-6215-
dc.identifier.isiWOS:000876282200006-
dc.publisher.placeLONDON-
dc.identifier.issnl1745-6215-

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