Skip to content

Urban Care Farming on Living Well and Productive Engagement of Older Adults

Effects of Urban Care Farming on Promoting Wellbeing and Productive Engagement for Older Adults: A Randomised Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06277583
Enrollment
137
Registered
2024-02-26
Start date
2024-03-15
Completion date
2025-05-22
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress, Psychological

Keywords

stress, quality of life, biopsychosocial

Brief summary

The goal of the randomized controlled trials is to learn about the effects of urban farming interventions on older adults' physical, mental, and social well-being of older adults aged 50 to 85 years. The main questions the study aims to answer are Q1. Would participants who have undergone the urban care farming intervention have lower stress levels compared to those who did not undergo the intervention? Q2. Would the quality of life and biopsychosocial factors of older adults who participate in the urban farming interventions be better before the intervention and compared to those who did not participate? Q3. Would running intervention programs as such demonstrate cost-effectiveness? Participants will be enrolled in 24 weekly lessons providing hands-on urban farming techniques, including physical activity, planting, and social interactions. Researchers will compare older participants with similar demographic profile to determine if the biological, psychological, and social factors are better for the intervention group.

Detailed description

The data collection consists of three sessions, before and after the 24-week intervention program, and 6 months post-intervention. Prior to the data collection, participants will be assessed for eligibility criteria and explained the detailed study procedures by trained research staff for informed consent. After completing the written informed consent, participants will be interviewed using detailed questionnaires relating to their health, nutrition, and dietary status, psychosocial measures, and undergo a series of physical examinations. These examinations include physical performance tests of mobility and gait, balance and strength, body measurements of weight, height, body mass index (BMI), waist-hip circumference, mid-upper-arm and calf circumference, blood pressure, and blood tests that will examine participants' clinical profile, biomarkers, and immunoassays. Participants will also be given Fitbit trackers to determine if they have improved their physical activity. Last, data collected will also include Functional near-infrared spectroscopy (fNIRS), a non-invasive procedure to determine the oxygenation levels of participants at rest and while doing some thinking activities. This data collection procedure will be conducted at baseline before the intervention and after the completion of the intervention. The intervention will include a weekly, 24-week urban farming program. Each weekly session is where participants will engage in outdoor and indoor horticultural activities ranging from fertilization, sowing, and watering, to transplanting, maintaining, and harvesting vegetables and herbs.

Interventions

BEHAVIORALUrban care farming

An intervention curriculum has been designed using horticulture therapy combined with urban farming techniques. The sessions will use plants and interaction with nature to engage and rehabilitate participants. Both the intervention and control group participants will undergo the intervention. But the intervention group will start with the urban care farming intervention first, and the control group will follow once the intervention group completes the program.

Sponsors

National University of Singapore
Lead SponsorOTHER
National Medical Research Council (NMRC), Singapore
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Waitlist controlled trials: Participants from both the intervention and waitlist control groups will undergo the intervention 6 months apart.

Eligibility

Sex/Gender
ALL
Age
50 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Willing to take part in the intervention * Agree for their data to be used for research purposes * Ambulant and able to carry out some tasks independently

Exclusion criteria

* Not willing to participate in the data collection (participants can opt not to answer some questions in the questionnaire but have to consent to the other data collection methods, e.g., Blood taking/test) * Refusal to give informed consent * Unable to give consent independently * Have a disability of the upper or lower body that limits their mobility * Have medical conditions which in the opinion of the research/investigative team that would compromise (or interfere with) their ability to participate in the study * Had a recent severe medical episode (e.g., heart attack)

Design outcomes

Primary

MeasureTime frameDescription
WHO Quality of Life Scale (WHOQOL-BREF)Baseline, 6 months, 12 monthsBrief version consisting of 26 QOL related questions developed by World Health Organisation. There are four domains, Physical, Psychological, Social relationships, and Environment. The minimum and maximum for each domain is 0 and 100 respectively, with higher scores being better outcome for each domain.

Secondary

MeasureTime frameDescription
Immuno-biomarkers: IL-1RA, IL-6, IL-8 (CXCL8), IL-10, IL-13, IL-17A (CTLA-8), MIP-3 beta (CCL19), SDF-1 alpha, MMP-3, MMP-9, MCP-1 (CCL2), and TNF alphaBaseline, 6 monthschanges in concentration of cytokines, chemokines and selected ageing and inflammatory markers in measured in pg/mL
Brief sense of community scale (BSCS)Baseline, 6 months, 12 months8-items measuring the dimensions of needs fulfillment, group membership, influence, and emotional connection. Composite scores with the average of the 8 items is computed, min 1 and max. 8, with higher scores showing greater sense of community.
Fried phenotype of frailtyBaseline, 6 months, 12 monthsFried frailty phenotype (FP) assesses physical frailty through five criteria: unintentional weight loss; weakness or poor handgrip strength; self-reported exhaustion; slow walking speed; and low physical activity. Total scores are classified into 3 categories: non-frail, pre-frail, and frail.
Lubben social network scale (LSNS-6)Baseline, 6 months, 12 monthsThis scale measure of social engagement including family and friends, min score of 6 and max. score of 30. A higher score indicating more social engagement and a cutoff of 12 points indicate risk of social isolation.
Functional near-infrared spectroscopyBaseline, 6 monthsBrain oxygenation levels measured in cerebral metabolic rate of oxygen (CMRO\^2).
EQ5DBaseline, 6 months, 12 monthsEQ5D-5L, a measure that consists five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. An utility score can be attached to the total score to determine the cost utility of the participants' quality of life. An utility score between 0 to 1 on the Singapore population will be derived.
MOCABaseline, 6 months, 12 monthsParticipants are scored following MOCA scoring criteria. Max. 30 points. Scores lower than 26 showed signs of cognitive impairment.
Brief resilience scaleBaseline, 6 months, 12 monthsResilience scale on a 5 points scale, strongly disagree to strongly agree, the higher the score, the greater resilience.
De jong Gierveld loneliness scaleBaseline, 6 months, 12 monthsMeasures emotional and/or social loneliness situation of respondents and adds up to a total loneliness score. the total loneliness score can be categorized into four levels: not lonely (score 0, 1 or 2), moderate lonely (score 3 through 8), severe lonely (score 9 or 10), and very severe lonely (score 11).
FitbitContinuous for 30 weeksSteps count
Body weight and heightBaseline, 6 months, 12 monthsMeasured in kilograms and metres respectively. Weight and height will be combined to report BMI in kg/m\^2
Fasting plasma glucose, HbA1cBaseline, 6 monthsmeasures average blood sugar levels over the past 3 months
Serum CreatinineBaseline, 6 monthsmeasures the level of creatinine in the blood
Attitude towards eating healthy foodBaseline, 6 months, 12 monthsAttitude of healthy eating (11-items) adapted from Saba et al 2019 (DOI: 10.1016/j.foodqual.2018.11.017). Composite score computed from the averaged measures will have a min of 1 and max of 5.
Waist and hip circumferenceBaseline, 6 months, 12 monthsMeasured in centimetres
Blood pressureBaseline, 6 months, 12 monthsMeasured in systolic and diastolic
Lipid panelBaseline, 6 monthsA lipid panel measures levels of various types of lipids (fats) in the blood. Measures HDL cholesterol (High-Density Lipoprotein) and LDL cholesterol (Low-Density Lipoprotein) and Triglycerides
Eating fruits and vegetables behaviorBaseline, 6 months, 12 monthsBehavior (8-items) towards eating fruits and vegetables developed for this study. Max. score of 10 and minimum score of 2 will be derived from this measurement.

Countries

Singapore

Contacts

PRINCIPAL_INVESTIGATORCynthia Chen, PhD

National University of Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026