Skip to content

Impact of Comprehensive Dietary Counseling on Dietary Quality, Mental Health, and Quality of Life in Older Adults

Impact of Comprehensive Dietary Counseling on Dietary Quality, Mental Health, and Quality of Life in Older Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03702335
Enrollment
50
Registered
2018-10-11
Start date
2018-11-13
Completion date
2021-11-30
Last updated
2021-09-02

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

Conditions

Aging, Age Problem, Age-related Cognitive Decline, Age-Related Atrophy

Keywords

Older adults, Dietary consultation, Mental health, Sleep quality, Dietary quality, Cardio-metabolic health

Brief summary

As a person ages, an incidence of mental distress such as depression and anxiety increases while the quality of life decreases. Singapore's population is aging rapidly and older adults may suffer from mental distress and deteriorated quality of life. Recent evidence suggests that good nutrition is essential for mental health and quality of life in older adults. Previous research reported that provision of nutrition education and cooking workshops to people with mental illness for 3 months achieved healthy dietary change and improved mental health. This proposed study aims to further assess the effect of comprehensive dietary counselling on dietary quality, cardio-metabolic, mental health, sleep quality, and quality of life through a 24-wk parallel intervention study in Singapore older adults. The investigators hypothesised that older adults who receive comprehensive dietary counselling will improve dietary quality, cardio-metabolic health, mental health, sleep quality, and quality of life when compared to older adults who do not receive comprehensive dietary counselling.

Detailed description

Fifty female Chinese older adults (aged 60+y) will be recruited with the expectation that ≥ 40 subjects will complete the study. This is a 24-wk parallel, single-bind, prospective study design with subjects randomly assigned to either receiving comprehensive dietary counselling (intervention group) or not receiving comprehensive dietary counselling (control group). Subjects in the intervention group will only receive comprehensive dietary counselling for first 12-wk and then they will be followed for another 12-wk without comprehensive dietary counselling. Subjects in the control group will be followed for 24-wk without any intervention. Dietary quality, mental health, sleep quality, daily physical activity and quality of life will be assessed and blood lipid-lipoproteins, glucose and insulin concentrations will be measured from the collected blood samples.

Interventions

Intervention group will be given a comprehensive dietary guidance on how to choose healthier options when eating out, as well as how to personally prepare a healthy meals.

Sponsors

National University of Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Able to give an informed consent 2. Age ≥60 years 3. No weight change \>3kg in the past 3 months 4. Not exercising vigorously over the past 3 months 5. Does not have any intestinal disorders, including lactose intolerance 6. No acute illness 7. Non-smoker 8. Non-vegetarian 9. Not drinking more than 2 alcoholic drinks/day 10. Not taking any lipid-lowering and blood pressure controlling medications less than 3 years

Exclusion criteria

1. Unable to give an informed consent 2. Age \< 60 years 3. Weight change \>3kg in the past 3 months 4. Exercises vigorously over the past 3 months 5. Have intestinal disorders, including lactose intolerence 6. Having acute illness 7. Smoking 8. Vegetarian 9. Drinking more than 2 alcoholic drinks/day 10. Taking lipid-lowering and blood pressure controlling medications less than 3 years

Design outcomes

Primary

MeasureTime frameDescription
Change in dietEvery 2 week for the first 12 weeks and every 4 weeks for the last 12 weeks (Week 0, week 2, week 4, week 6, week 8, week 10, week 12, week 16, week 20, week 24)Dietary assessment, 3-day food record (participant)
Change in mental health statusEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Mental Health Questionnaire - Consisting of basic health screen recording anthropometric measurements, visual functioning questionnaire scale (1; Good, 2; Acceptable, 3; Poor), Lifestyle (0; Never, 1; 1-3 times/month, 2; 1-3 times/week, 3; 4-6 times/week, 4; daily), depression scale (Yes or no questionnaire)
Change in quality of lifeEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Quality of Life Questionnaire * Subjective scale rating (1; very dissatisfied, 2; dissatisfied, 3; neither satisfied not dissatisfied, 4; satisfied, 5; very satisfied) assessing quality of life, health and other areas of life.
Change in sleep qualityEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Pittsburgh Sleep Quality Assessment (PSQI) - Recall based questionnaire assessing sleep habits for the past one month only which includes sleeping timing habits and quality of sleep (Very good, Fairly good, Fairly bad and very bad)

Secondary

MeasureTime frameDescription
Change in total cholesterolEvery 12 weeks (Week 0, week 12, and week 24)Total cholesterol (mmol/l)
Change in high-density lipoprotein cholesterolEvery 12 weeks (Week 0, week 12, and week 24)High-density lipoprotein cholesterol (mmol/l)
Change in low-density lipoprotein cholesterolEvery 12 weeks (Week 0, week 12, and week 24)Low-density lipoprotein cholesterol (mmol/l)
Change in dietEvery 12 weeks (Week 0, week 12 and week 24)Dietary Assessment, 3-day food record (Participant's family member)
Change in blood glucose concentrationEvery 12 weeks (Week 0, week 12, and week 24)Blood glucose concentration
Change in blood insulin concentrationEvery 12 weeks (Week 0, week 12, and week 24)Blood insulin concentration
Change in daily physical activityDaily (Week 0 to week 24)Tracked with an electronic activity tracker
Change in total triglycerideEvery 12 weeks (Week 0, week 12, and week 24)Total triglyceride (mmol/l)
Change in weightEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Weight (kg)
Change in waist circumferenceEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Waist Circumference (cm)
Change in blood pressureEvery 4 weeks (Week 0, week 4, week 8, week 12, week 16, week 20 and week 24)Systolic and diastolic blood pressure (mmHg) after a 10 hour overnight fast

Countries

Singapore

Contacts

Primary ContactJung Eun Kim, PhD, RD
fstkje@nus.edu.sg65161136
Backup ContactJasmine Low, BSc (Hons)
jasmine.low@u.nus.edu94510860

Outcome results

None listed

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