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临床试验/NCT03576170
NCT03576170已完成不适用

Investigate the Efficacy and Effectiveness of Aromatherapy for the Management of Behavioral and Psychological Symptoms of Dementia

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2017年11月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
112
试验地点
1
主要终点
Chinese Version of the Neuropsychiatric Inventory (NPI)

研究概览

简要总结

In recent decades, following an increased longevity in Hong Kong, there is a drastic increase in the prevalence chronic conditions, including dementia. Behavioral and psychological symptoms of dementia (BDSP) seem to be the main reasons of suffering for many older adults. This condition does not only pose a burden to the whole family but also the healthcare system.

While conventional treatment of BPSD using pharmacotherapy and non-pharmacological treatments has been effective for managing symptoms, owing to the adverse side effects caused by anti-psychotic drugs and the short effective period incurred by non-pharmacological interventions, development of alternative and non-pharmacological approaches for the management of behavioral disturbances and pain is of urgent need. Research has shown that aromatherapy (both administered through inhalation and therapeutic massage) has been effective in reducing behavioral disturbances of dementia patients. These findings support the premise that aromatherapy and the investigators hope to provide further evidence to support the use of aromatherapy as an evidence-based mainstream intervention for reducing behavioral and psychological symptoms of dementia (BPSD).

Whilst there is sufficient evidence to support the effectiveness of aromatherapy, few studies compared the effectiveness of the use of aromatherapy by inhalation and/or therapeutic massage. The investigators aim to address the above research gaps on the clinical application of aromatherapy on BPSD, with a focus on comparing the differential effectiveness between administration by inhalation and administration by therapeutic massage. The proposed research aims to (1) test the efficacy and effectiveness of aromatherapy on the symptom management of BPSD in older adults; (2) compare the effects of aromatherapy-scent (i.e., inhalation) and aromatherapy-touch (i.e., therapeutic massage) in older adults with BPSD. This study also explores the benefits of aromatherapy on cognitive functioning, functional performance and social engagement as secondary outcomes.

A randomized, controlled, and single blinded trial is proposed. 120 older adults with BPSD will be randomly assigned to aroma inhalation (intervention), aroma-touch or wait-list (control) treatments. The primary outcomes measured are a caregiver-rated inventory of agitated behaviors and abnormalities of mood and psychotic phenomenal, cognitive functioning, functional performance and social engagement (secondary outcome) will be assessed three time points the study hypotheses are supported, the findings will provide empirical support for a treatment option that could improve psychological well-being and also improve cognitive functioning, functional performance, and social engagement of older adults.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 60 years of age or older
  • have a CMMSE score below 18 if illiterate, 19 if they have 1-2 years of education, and 20 if they had more than 2 years of education
  • reported to have BPSD;
  • willing to participate in the research, with informed consent signed by their guardian or carer.

排除标准

  • allergic to essential oils
  • refused to give consent
  • over-sensitive to tactile stimulation
  • have a history of kidney and liver disease
  • have ever had an epileptic seizure.

研究组 & 干预措施

aromatherapy-scent

Active Comparator

干预措施: aromatherapy (Other)

aromatherapy-touch

Active Comparator

干预措施: aromatherapy (Other)

wait-list control

No Intervention

结局指标

主要结局

Chinese Version of the Neuropsychiatric Inventory (NPI)

时间窗: baseline, 2-months after intervention and after the completion of the intervention in four months

It is used to assess the changes of the abnormalities of mood and psychotic phenomena among three times points (baseline, 2-months after intervention and after the completion of the intervention) in four months. If the response to the domain question is "No", the informant goes to the next question. If "Yes", the informant then rates both the Severity of the symptoms present within the last month on a 3-point scale and the associated impact of the symptom manifestations on them (i.e. Caregiver Distress) using a 5-point scale. The NPI-Q provides symptom Severity and Distress ratings for each symptom), and total Severity and Distress scores reflecting the sum of individual domain scores ranging from 0 to 36 and ranging from 0 to 60 respectively.

Chinese Version of the Cohen- Mansfield Agitation Inventory (CMAI)

时间窗: baseline, 2-months after intervention and after the completion of the intervention in four months

It is a care-giver rated inventory to assess agitation in elderly persons and records the frequency of occurrence of BDSP at different period of time and thus can be used for assessing the changes among three times points (baseline, 2-months after intervention and after the completion of the intervention) in four months. It includes descriptions of 29 agitated behaviors, and each is rated on a 7-point scale of frequency. The total scores range from 29 points to 203 points, a higher score of CMAI indicates more frequent agitation behaviors.

次要结局

  • Cantonese Version of the Mini-mental State Examination (CMMSE)(baseline, 2-months after intervention and after the completion of the intervention in four months)
  • Chinese Version of the Index of Social Engagement(ISE)(baseline, 2-months after intervention and after the completion of the intervention in four months)
  • Chinese Version of the Barthel Index-100(baseline, 2-months after intervention and after the completion of the intervention in four months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

TSANG Hector Wing-Hong

Professor and Head Department of Rehabilitation Science

The Hong Kong Polytechnic University

研究点 (1)

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