The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design
<p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholineste...
Ausführliche Beschreibung
Autor*in: |
Andersen Fred [verfasserIn] Viitanen Matti [verfasserIn] Halvorsen Dag S [verfasserIn] Straume Bjørn [verfasserIn] Wilsgaard Tom [verfasserIn] Engstad Torgeir A [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2012 |
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Übergeordnetes Werk: |
In: BMC Neurology - BMC, 2003, 12(2012), 1, p 59 |
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Übergeordnetes Werk: |
volume:12 ; year:2012 ; number:1, p 59 |
Links: |
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DOI / URN: |
10.1186/1471-2377-12-59 |
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Katalog-ID: |
DOAJ054410290 |
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245 | 1 | 4 | |a The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design |
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520 | |a <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< | ||
650 | 4 | |a Alzheimer’s disease | |
650 | 4 | |a Symptomatic treatment | |
650 | 4 | |a Postponement of cognitive deterioration | |
653 | 0 | |a Neurology. Diseases of the nervous system | |
700 | 0 | |a Viitanen Matti |e verfasserin |4 aut | |
700 | 0 | |a Halvorsen Dag S |e verfasserin |4 aut | |
700 | 0 | |a Straume Bjørn |e verfasserin |4 aut | |
700 | 0 | |a Wilsgaard Tom |e verfasserin |4 aut | |
700 | 0 | |a Engstad Torgeir A |e verfasserin |4 aut | |
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10.1186/1471-2377-12-59 doi (DE-627)DOAJ054410290 (DE-599)DOAJ5e9c4ca3c2354bf89d2cf7010138aace DE-627 ger DE-627 rakwb eng RC346-429 Andersen Fred verfasserin aut The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< Alzheimer’s disease Symptomatic treatment Postponement of cognitive deterioration Neurology. Diseases of the nervous system Viitanen Matti verfasserin aut Halvorsen Dag S verfasserin aut Straume Bjørn verfasserin aut Wilsgaard Tom verfasserin aut Engstad Torgeir A verfasserin aut In BMC Neurology BMC, 2003 12(2012), 1, p 59 (DE-627)326643664 (DE-600)2041347-6 14712377 nnns volume:12 year:2012 number:1, p 59 https://doi.org/10.1186/1471-2377-12-59 kostenfrei https://doaj.org/article/5e9c4ca3c2354bf89d2cf7010138aace kostenfrei http://www.biomedcentral.com/1471-2377/12/59 kostenfrei https://doaj.org/toc/1471-2377 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2012 1, p 59 |
spelling |
10.1186/1471-2377-12-59 doi (DE-627)DOAJ054410290 (DE-599)DOAJ5e9c4ca3c2354bf89d2cf7010138aace DE-627 ger DE-627 rakwb eng RC346-429 Andersen Fred verfasserin aut The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< Alzheimer’s disease Symptomatic treatment Postponement of cognitive deterioration Neurology. Diseases of the nervous system Viitanen Matti verfasserin aut Halvorsen Dag S verfasserin aut Straume Bjørn verfasserin aut Wilsgaard Tom verfasserin aut Engstad Torgeir A verfasserin aut In BMC Neurology BMC, 2003 12(2012), 1, p 59 (DE-627)326643664 (DE-600)2041347-6 14712377 nnns volume:12 year:2012 number:1, p 59 https://doi.org/10.1186/1471-2377-12-59 kostenfrei https://doaj.org/article/5e9c4ca3c2354bf89d2cf7010138aace kostenfrei http://www.biomedcentral.com/1471-2377/12/59 kostenfrei https://doaj.org/toc/1471-2377 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2012 1, p 59 |
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10.1186/1471-2377-12-59 doi (DE-627)DOAJ054410290 (DE-599)DOAJ5e9c4ca3c2354bf89d2cf7010138aace DE-627 ger DE-627 rakwb eng RC346-429 Andersen Fred verfasserin aut The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< Alzheimer’s disease Symptomatic treatment Postponement of cognitive deterioration Neurology. Diseases of the nervous system Viitanen Matti verfasserin aut Halvorsen Dag S verfasserin aut Straume Bjørn verfasserin aut Wilsgaard Tom verfasserin aut Engstad Torgeir A verfasserin aut In BMC Neurology BMC, 2003 12(2012), 1, p 59 (DE-627)326643664 (DE-600)2041347-6 14712377 nnns volume:12 year:2012 number:1, p 59 https://doi.org/10.1186/1471-2377-12-59 kostenfrei https://doaj.org/article/5e9c4ca3c2354bf89d2cf7010138aace kostenfrei http://www.biomedcentral.com/1471-2377/12/59 kostenfrei https://doaj.org/toc/1471-2377 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2012 1, p 59 |
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10.1186/1471-2377-12-59 doi (DE-627)DOAJ054410290 (DE-599)DOAJ5e9c4ca3c2354bf89d2cf7010138aace DE-627 ger DE-627 rakwb eng RC346-429 Andersen Fred verfasserin aut The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< Alzheimer’s disease Symptomatic treatment Postponement of cognitive deterioration Neurology. Diseases of the nervous system Viitanen Matti verfasserin aut Halvorsen Dag S verfasserin aut Straume Bjørn verfasserin aut Wilsgaard Tom verfasserin aut Engstad Torgeir A verfasserin aut In BMC Neurology BMC, 2003 12(2012), 1, p 59 (DE-627)326643664 (DE-600)2041347-6 14712377 nnns volume:12 year:2012 number:1, p 59 https://doi.org/10.1186/1471-2377-12-59 kostenfrei https://doaj.org/article/5e9c4ca3c2354bf89d2cf7010138aace kostenfrei http://www.biomedcentral.com/1471-2377/12/59 kostenfrei https://doaj.org/toc/1471-2377 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2012 1, p 59 |
allfieldsSound |
10.1186/1471-2377-12-59 doi (DE-627)DOAJ054410290 (DE-599)DOAJ5e9c4ca3c2354bf89d2cf7010138aace DE-627 ger DE-627 rakwb eng RC346-429 Andersen Fred verfasserin aut The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< Alzheimer’s disease Symptomatic treatment Postponement of cognitive deterioration Neurology. Diseases of the nervous system Viitanen Matti verfasserin aut Halvorsen Dag S verfasserin aut Straume Bjørn verfasserin aut Wilsgaard Tom verfasserin aut Engstad Torgeir A verfasserin aut In BMC Neurology BMC, 2003 12(2012), 1, p 59 (DE-627)326643664 (DE-600)2041347-6 14712377 nnns volume:12 year:2012 number:1, p 59 https://doi.org/10.1186/1471-2377-12-59 kostenfrei https://doaj.org/article/5e9c4ca3c2354bf89d2cf7010138aace kostenfrei http://www.biomedcentral.com/1471-2377/12/59 kostenfrei https://doaj.org/toc/1471-2377 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2012 1, p 59 |
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effect of stimulation therapy and donepezil on cognitive function in alzheimer’s disease. a community based rct with a two-by-two factorial design |
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The effect of stimulation therapy and donepezil on cognitive function in Alzheimer’s disease. A community based RCT with a two-by-two factorial design |
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<p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< |
abstractGer |
<p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< |
abstract_unstemmed |
<p<Abstract</p< <p<Background</p< <p<Progressive neurodegeneration in Alzheimer’s disease (AD) induces cognitive deterioration, and there is controversy regarding the optimal treatment strategy in early AD. Stimulation therapy, including physical exercise and cholinesterase inhibitors are both reported to postpone cognitive deterioration in separate studies. We aimed to study the effect of stimulation therapy and the additional effect of donepezil on cognitive function in early AD.</p< <p<Method</p< <p<Design: A two-by-two factorial trial comprising stimulation therapy for one year compared to standard care to which a randomized double-blinded placebo controlled trial with donepezil was added.</p< <p<Setting: Nine rural municipalities in Northern Norway.</p< <p<Participants: 187 participants 65 years and older with a recent diagnosis of mild or moderate AD were included in the study of which 146 completed a one-year follow-up. INTERVENTIONS: In five municipalities the participants received stimulation therapy whereas participants in four received standard care. All participants were randomised double-blindly to donepezil or placebo and tested with three different cognitive tests four times during the one-year study period.</p< <p<Main outcome: Changes in MMSE sum score.</p< <p<Secondary outcome: Changes in ADAS-Cog and Clock Drawing Test.</p< <p<Results</p< <p<MMSE scores remained unchanged amongst AD participants receiving stimulation therapy and those receiving standard care. The results were consistent for ADAS-Cog and Clock Drawing Test. No time trend differences were found during one-year follow-up between groups receiving stimulation therapy versus standard care or between donepezil versus placebo.</p< <p<Conclusion</p< <p<In rural AD patients non-pharmacological and pharmacological therapy did not improve outcome compared with standard care but all groups retained cognitive function during one year follow-up. Other studies are needed to confirm these results.</p< <p<Trial registration</p< <p<ClinicalTrials.gov (Identifier: NCT00443014). EudraCT database (no 2004-002613-37).</p< |
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