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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

Tracking Information
First Submitted Date  ICMJE February 5, 2017
First Posted Date  ICMJE February 7, 2017
Last Update Posted Date February 7, 2017
Actual Study Start Date  ICMJE January 1, 2017
Estimated Primary Completion Date August 1, 2019   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: February 5, 2017)
  • 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.
  • 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.
  • 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.
  • 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.
  • 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
  • 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.
Original Primary Outcome Measures  ICMJE Same as current
Change History No Changes Posted
Current Secondary Outcome Measures  ICMJE
 (submitted: February 5, 2017)
  • 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).
  • 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.
  • 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.
  • 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).
  • 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.
  • 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.
  • 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)
  • 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.
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Effects of Horticultural Therapy on Elderly at Risk of Cognitive Decline
Official Title  ICMJE Effects of Horticultural Therapy on Elderly at Risk of Cognitive Decline
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.

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.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Condition  ICMJE
  • Horticultural Therapy
  • Dementia
Intervention  ICMJE 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.
Study Arms  ICMJE
  • Experimental: Horticultural Therapy
    Horticultural Therapy will consists of 1 hour sessions, weekly for 9 months, to engage subjects in gardening-based activities.
    Intervention: Behavioral: Horticultural Therapy
  • 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.
    Intervention: Behavioral: Horticultural Therapy
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Unknown status
Estimated Enrollment  ICMJE
 (submitted: February 5, 2017)
100
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE December 1, 2019
Estimated Primary Completion Date August 1, 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

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
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 60 Years to 100 Years   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Singapore
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03045718
Other Study ID Numbers  ICMJE 2016/00949
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: No
Plan Description: Individual data will not be shared, in the interests of subject confidentiality
Current Responsible Party National University Hospital, Singapore
Original Responsible Party Same as current
Current Study Sponsor  ICMJE National University Hospital, Singapore
Original Study Sponsor  ICMJE Same as current
Collaborators  ICMJE
  • National Parks Board, Singapore
  • Ministry of Health, Singapore
  • Ministry of National Development, Singapore
Investigators  ICMJE
Principal Investigator: Hong Yee Tan, MMed(Psy) Associate Consultant
PRS Account National University Hospital, Singapore
Verification Date February 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP