Effects of Community-center Based Dietary Intervention on Frailty Prevention and Regression in the Elderly.

Sponsor
Academia Sinica, Taiwan (Other)
Overall Status
Terminated
CT.gov ID
NCT05129163
Collaborator
(none)
219
1
2
15.8
13.9

Study Details

Study Description

Brief Summary

Recent interventional studies have shown that frailty can be improved by modifying dietary quality. In this study, a set of nutrition-centric health promotion activities was developed in accordance with the Taiwanese Daily Food Guide for elderly participants of the community centers to improve their nutrition in everyday practice and examined the efficacy of these activities on slowing down the development or regression of frailty. The study was a cluster-randomized controlled trial. Recruited community centers were randomly assigned into either the control or the intervention group. The intervention period lasted for 3 months. Both the control and intervention groups received weekly one-hour group exercise training. The intervention group had an additional weekly one-hour group nutrition session. The intervention programs included: (a) training on-site staffs to use motivational interview techniques to communicate, to estimate participant's energy requirements, and to learn how to provide proper amounts of foods to individual elderlies, (b) nutrition grouped activities on ①know my plate, ②wholegrains, ③drinking teas with dairy, and nuts, ④novel ways to eat fruit and vegetables, ⑤healthy breakfast ideas. In the first month, participants were intervened with the activities laid out above; in the second month, participants were intervened with qualitative discussions on dietary changes; in the third month, participants were intervened with designed activities that helped break down barriers in order to establish a long-term change in dietary habits. Improvement in nutritional status was the primary outcome. Secondary outcomes included frailty scores, physical performance, and mental health. The measurements were performed at baseline, 3 months, and 6 months.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise
  • Behavioral: Nutrition activities
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
219 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Associations Between Various Geriatric Syndromes and Nutrition Status and Dietary Pattern in Elderly
Actual Study Start Date :
Aug 27, 2018
Actual Primary Completion Date :
Dec 20, 2019
Actual Study Completion Date :
Dec 20, 2019

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Exercise

The control group received weekly one-hour group exercise training for 3 months.

Behavioral: Exercise
The group exercise training was held in each community center. The group exercise training contained aerobic exercise, complex physical fitness exercise, muscle training, and balance and coordination training.

Experimental: Exercise and nutrition

The intervention group had weekly one-hour group exercise training the same as the control and an additional weekly one-hour group nutrition session for 3 months.

Behavioral: Exercise
The group exercise training was held in each community center. The group exercise training contained aerobic exercise, complex physical fitness exercise, muscle training, and balance and coordination training.

Behavioral: Nutrition activities
The intervention programs included: (a) training on-site staffs to use motivational interview techniques to communicate, to estimate participant's energy requirements, and to learn how to provide proper amounts of foods to individual elderlies, (b) nutrition grouped activities on ①know my plate, ②wholegrains, ③ drinking teas with dairy, and nuts, ④novel ways to eat fruit and vegetables, ⑤healthy breakfast ideas. In the first month, participants were intervened with the activities laid out above; in the second month, participants were intervened with qualitative discussion on elders' dietary changes; in the third month, participants were intervened with designed activities that helped break down barriers in order to establish a long-term change in dietary habits.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in intake frequency (portion per day) on the six food groups at months 3 and 6. [Baseline, Month 3 and Month 6]

    The six food groups include: Whole grains and starchy vegetables Protein foods: soy beans, fish, eggs, and meat Vegetables Fruits Dairy Oils, nuts and seeds

  2. Change from baseline in the ratios of concentration on urinary nutritional biomarkers at months 3 and 6. [Baseline, Month 3 and Month 6]

    The concentrations of the following urinary nutritional biomarkers were determined: urinary urea nitrogen (mg/dL), urinary calcium (mg/dl), urinary potassium (mmol/L), urinary magnesium (mg/dL), and urinary creatinine (mg/dL). The urinary urea nitrogen to creatinine ratios, urinary calcium to creatinine ratios, urinary potassium to creatinine ratios, and urinary magnesium to creatinine ratios was estimated at baseline, moths 3 and 6.

  3. Change from baseline in frailty status at months 3 and 6. [Baseline, Month 3 and Month 6]

    Frailty status was defined using modified Linda Fried criteria with cutoff points from the investigators' previous intervention studies. Five frail phenotypes were assigned: (1) unintentional weight loss, (2) self-reported exhaustion, (3) weak grip strength, (4) slow gait speed, and (5) low level of physical activity. To estimate frailty, participants scored 1 point from each phenotype if any of these were satisfied; a maximum score of five was possible. Participants were classified by their point scores as follows: 'robust' for 0 point; 'pre-frail' for 1 or 2 points; and 'frail' for ≥3.

Secondary Outcome Measures

  1. Change from baseline in the score of digit span at months 3 and 6. [Baseline, Month 3 and Month 6]

    A digit span task is used to measure working memory's number storage capacity. Subjects are read a sequence of numbers and asked to repeat the same sequence back to the examiner in order (forward span) or in reverse order (backward span). The score is the length of the longest correctly repeated sequence. The maximum number of digits in a sequence is 9 and the minimum number of digits in a sequence is 2. The higher scores mean a better outcome.

  2. Change from baseline in the scores on the Geriatric Depression Scale at months 3 and 6. [Baseline, Month 3 and Month 6]

    The Geriatric Depression Scale (GDS) is a self-report measure of depression in older adults. Scores of 0-4 are considered normal, depending on age, education, and complaints; 5-8 indicate mild depression; 9-11 indicate moderate depression; and 12-15 indicate severe depression.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged 65 years or older

  • Able to walk independently for 14 meters within 1 minute

  • Willing to sign the informed consent

Exclusion Criteria:
  • Under dietary control by doctors' instructions

  • With mental illness, mental disorders, or unable to communicate

  • With severe diseases such as under treatments for cancer

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institute of Biomedical Sciences, Academia Sinica Taipei Taiwan 115

Sponsors and Collaborators

  • Academia Sinica, Taiwan

Investigators

  • Principal Investigator: Wen-Harn Pan, PhD, Academia Sinica, Taiwan

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Wen-Harn Pan, Distinguished Research Fellow, Academia Sinica, Taiwan
ClinicalTrials.gov Identifier:
NCT05129163
Other Study ID Numbers:
  • AS-IRB01-16057
First Posted:
Nov 22, 2021
Last Update Posted:
Jan 25, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 25, 2022