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Effects of Horticultural Therapy on Elderly at Risk of Cognitive Decline

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03045718
Recruitment Status : Unknown
Verified February 2017 by National University Hospital, Singapore.
Recruitment status was:  Enrolling by invitation
First Posted : February 7, 2017
Last Update Posted : February 7, 2017
Sponsor:
Collaborators:
National Parks Board, Singapore
Ministry of Health, Singapore
Ministry of National Development, Singapore
Information provided by (Responsible Party):
National University Hospital, Singapore

Brief Summary:

The objective of this study is to determine whether horticultural therapy would improve the psychological well-being older adults who are at risk of memory (cognitive) decline. 100 elderly subjects who are at risk of cognitive decline will be randomized into the active horticultural therapy or to the waitlist control group. Sessions will be conducted weekly for 9 months, and participants will be assessed at 3 time-points: at the start of the study, at 3 months and at 9 months.

It is hypothesized that participants who undergo horticultural therapy will perform better on neuropsychological tests when compared to control, and that they will have improved psychological well-being and functional outcomes.


Condition or disease Intervention/treatment Phase
Horticultural Therapy Dementia Behavioral: Horticultural Therapy Not Applicable

Detailed Description:

Study participants comprise of community-dwelling elderly who are at risk of developing dementia, and will be selected from consenting participants from an existing community cognitive screening program.

This is an intervention study where 100 subjects will be randomized into an active horticultural therapy group, or a waitlist control group. Baseline demographic data will be collected at the start of the study. Assessments will be done at the start, at 3 months and at 6 months, which will include neuropsychological tests of cognitive functioning, psychological tests for depression and anxiety, assessment of psychosocial well-being, and tests of functional status.

The Horticultural Therapy intervention will be delivered by trained facilitators at the Therapeutic Garden at Hort Park, and consists of 1 hour sessions weekly for 9 months. The Horticultural Therapy program is designed to stimulate the senses through interaction with the tasks and the environment, promote social interaction and also to promote a sense of self-worth through completion of projects. It encompasses a range of activities including general gardening and also project-based craft activities.

The control group will be placed on a waiting list and only be contacted for assessments. They will receive intervention after the active treatment group at a later date.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Effects of Horticultural Therapy on Elderly at Risk of Cognitive Decline
Actual Study Start Date : January 1, 2017
Estimated Primary Completion Date : August 1, 2019
Estimated Study Completion Date : December 1, 2019

Arm Intervention/treatment
Experimental: Horticultural Therapy
Horticultural Therapy will consists of 1 hour sessions, weekly for 9 months, to engage subjects in gardening-based activities.
Behavioral: Horticultural Therapy
The Horticultural Therapy intervention will be delivered by trained facilitators at the Therapeutic Garden at Hort Park, and consists of 1 hour sessions weekly for 9 months. The Horticultural Therapy program is designed to stimulate the senses through interaction with the tasks and the environment, promote social interaction and also to promote a sense of self-worth through completion of projects. It encompasses a range of activities including general gardening and also project-based craft activities.

Waitlist Control
The control group will be placed on a waiting list and only be contacted for assessments. They will receive the same Horticultural Therapy intervention after the active treatment group at a later date.
Behavioral: Horticultural Therapy
The Horticultural Therapy intervention will be delivered by trained facilitators at the Therapeutic Garden at Hort Park, and consists of 1 hour sessions weekly for 9 months. The Horticultural Therapy program is designed to stimulate the senses through interaction with the tasks and the environment, promote social interaction and also to promote a sense of self-worth through completion of projects. It encompasses a range of activities including general gardening and also project-based craft activities.




Primary Outcome Measures :
  1. Changes in Clinical Dementia Rating (CDR) at baseline and at 9 months [ Time Frame: Baseline, 9 months ]
    Clinical Dementia Rating (CDR ) is a 5-point scale used to characterize six domains of cognitive and functional performance applicable to Alzheimer disease and related dementias: Memory, Orientation, Judgment & Problem Solving, Community Affairs, Home & Hobbies, and Personal Care.

  2. Changes in Colour Trails Tests (CTT) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Colour Trails Tests (CTT) 1 and 2 assesses sustained attention and sequencing.

  3. Changes in Digit Span Task scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Digit Span Task, which consists of a Digit Span Forward (DSF) and a Digit Span Backward (DSB) task is used to assess attention and verbal working memory.

  4. Changes in Rey Auditory Verbal Learning Test (RAVLT) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Rey Auditory Verbal Learning Test (RAVLT) evaluates declarative verbal learning and memory.

  5. Changes in Block Design scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Block Design is a subtest that is administered as part of several of the Wechsler Intelligence tests, and it primarily measures visual-spatial and organizational processing abilities, as well as non-verbal problem-solving skills

  6. Changes in Semantic Verbal Fluency scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Semantic Verbal Fluency assess lexical knowledge and semantic memory organization.


Secondary Outcome Measures :
  1. Changes in Zung Self-Rating Depression Scale (SDS) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The SDS (Zung, 1965) is a 20-item quantitative measurement of symptoms of depression. Participants rate each item regarding how they felt during the week preceding using a 4-point scale that ranges from 1 (a little of the time) to 4 (most of the time). A total raw score computed by summing the scores on the individual items will be converted into a percentage (the SDS index); the higher the SDS index, the greater the severity of depressive symptoms. Several studies have established the SDS as a reliable and valid instrument for measuring depressive symptoms (Biggs et al., 1978; Gabrys and Peters, 1985; Agrell and Dehlin, 1989).

  2. Changes in Zung Self-Rating Anxiety Scale (SAS) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The SAS (Zung, 1971) will be used to measure anxiety of the participants in the preceding week. It is a 20-item self-report assessment designed to measure anxiety levels, based on cognitive, autonomic, motor and central nervous system symptoms. Each question is scored on a Likert-type scale of 1-4 (a little of the time) to (most of the time). Some questions are negatively worded to avoid the problem of set response. Overall assessment is done by total score. The total raw scores range from 20-80. The raw score then needs to be converted to an "Anxiety Index" score; the higher the SAS index, the greater the severity of depressive symptoms.

  3. Changes in Ryff's Scales of Psychological Well-being scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The Ryff Scales of Psychological Well-Being (Ryff and Singer, 1998) is an 18-item questionnaire which reflects the six areas of psychological well-being: autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, and self-acceptance. Respondents rate statements on a scale of 1 to 6, with 1 indicating strong disagreement and 6 indicating strong agreement.

  4. Changes in Friendship Scale (FS) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    Social connectedness scale will be measured using the Friendship Scale (Hawthorne, 2006). It is a 6-item questionnaire that measures both social isolation and social connectedness. Participants were asked to rate the frequency in which each statement describes them during the past four weeks on a 5-point Likert scale ranging from 0 (almost always) to 5 (not at all). Total scores were computed by summing the scores on the individual items and ranged from 0 to 24, with higher scores indicating higher level of social connectedness. The Friendship Scale was developed as a short, user-friendly, stand alone scale measuring perceived social isolation. It was validated with older adults with excellent internal structures, reliability and validity (Hawthorne, 2006; Hawthorne, 2008).

  5. Changes in EuroQol Five Dimensions Questionaire (ED-5D-3L) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The E5-5D-3L is a standardized instrument for measuring general health status, which consists of 5 questions and a visual analog scale - which is a self-rating scale ranging from zero (0) to one hundred (100) to indicate the perceived health state from worst to best respectively.

  6. Changes in the Modified Barthel Index (MBI) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The MBI is an instrument used to assess the performance in Activities of Daily Living, and consists of 10 variables that reflect activities of daily living and mobility used to monitor functional status.

  7. Changes in the Instrumental Activities of Daily Living Scale (IADL) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The IADL Scale is used to assess more complex activities of daily living necessary for functioning in community living, such as handling finances and food preparation. It consists of 8 items which are summarily scored from zero (low functioning) to 8 (high functioning)

  8. Changes in the Pittsburgh Sleep Quality Index (PSQI) scores at baseline, 3 months and 9 months [ Time Frame: Baseline, 3 months, 9 months ]
    The PSQI is a self-report questionnaire that assesses sleep quality, and consists of 19 individual items, creating 7 components that produce one global score, and takes 5-10 minutes to complete.



Information from the National Library of Medicine

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Ages Eligible for Study:   60 Years to 100 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

1. Community-living elderly aged 60 years and above, AND 2.

  1. Mild Cognitive Impairment based on clinical history and neuropsychological test scores (Z score <0 and >-1.5), OR
  2. Subjective Memory Impairment based on self-report, OR (C) 2 or more risk factors for dementia such as family history, cerebrovascular disease, and cardiovascular risk factors

Exclusion Criteria:

  1. Existing diagnosis of dementia, OR
  2. Comorbid major mental illness (such as Major Depressive Disorder and Psychosis), OR
  3. Severe or unstable life-limiting medical illness, OR
  4. Severe physical impairment precluding participation in Horticultural Therapy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03045718


Locations
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Singapore
National University Hospital
Singapore, Singapore
Sponsors and Collaborators
National University Hospital, Singapore
National Parks Board, Singapore
Ministry of Health, Singapore
Ministry of National Development, Singapore
Investigators
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Principal Investigator: Hong Yee Tan, MMed(Psy) Associate Consultant
Publications:
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Responsible Party: National University Hospital, Singapore
ClinicalTrials.gov Identifier: NCT03045718    
Other Study ID Numbers: 2016/00949
First Posted: February 7, 2017    Key Record Dates
Last Update Posted: February 7, 2017
Last Verified: February 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Individual data will not be shared, in the interests of subject confidentiality

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by National University Hospital, Singapore:
Horticultural Therapy
Dementia
Randomized Controlled Trial
Elderly
Prevention
Additional relevant MeSH terms:
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Dementia
Cognitive Dysfunction
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurocognitive Disorders
Mental Disorders
Cognition Disorders