ClinicalTrials.Veeva

Menu

Evaluation Study for the Chef Anchor 3.0 Program

The University of Hong Kong (HKU) logo

The University of Hong Kong (HKU)

Status

Enrolling

Conditions

Mild Cognitive Impairment
Dementia

Treatments

Other: 10-week programme

Study type

Interventional

Funder types

Other

Identifiers

NCT06572748
EA240323

Details and patient eligibility

About

Objectives:

  1. (Primary)To estimate the potential effects of the cooking program on the people with MCI/dementia and their informal caregivers;
  2. To investigate if the potential effects can be maintained after the completion of the program.

Study design and participants:

A convenience sample of 68 pair older adults with MCI/dementia and their informal caregivers from the Chef Anchor 3.0 Programme will be referred to the research team. Overall, participants will be assigned to intervention group and waitlist control group in a ratio of 1:1. Allocation will take into account the participants' availability and the programme capacity. Assessors of outcomes and data analyst will be blinded throughout the whole study.

During the first 10 weeks, the intervention group will undergo the 10-week programme in the "Chef Anchor 3.0", while no activity for the waitlist control group. Then, from week 10 to 20, the waitlist control group will attend the same 10-week programme.

Measurements:

Main outcome measures for people with MCI/dementia will include confidence in cooking (Primary), cooking capability, satisfaction with autonomy in cooking, Satisfaction with meal choices, Worried about future cooking ability and meal choices, cognitive function, self-reported appetite, psychological well-being, family harmony and satisfaction, as well as self-rated health.

Outcome measures for informal caregivers will include confidence in care recipient' s cooking, worried about future cooking ability and meal choices of care recipient, caregiver burden, psychological well-being, family harmony and satisfaction, as well as self-rated health.

Other measures will include attendance rate, home practice rate, drop-out rate, programme satisfaction, and recommendation to others.

Hypotheses

  1. The confidence in cooking, cooking capability, satisfaction with autonomy in cooking, satisfaction with meal choices, worried about future cooking ability and meal choices, cognitive function, self-reported appetite, psychological well-being, family satisfaction, and self-rated health of older adults with MCI/dementia would improve after the programme;
  2. The confidence in care recipient's cooking, worried about future cooking ability and meal choices of care recipient, psychological well-being, family satisfaction, caregiver burden, and self-rated health of informal caregivers would improve after the programme;
  3. The 10-week programme is acceptable for the most of older adults with MCI/dementia and their informal caregivers.

Enrollment

136 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

i. Aged 60 or above;

ii. Diagnosed by medical doctor has having MCI/dementia as reported by the older adults or their informal caregivers, or with reported subjective decline of cognitive function and with 5-min MoCA score ≤7th age- and education-specific percentile (Wong et al., 2015);

iii. Ability to follow simple instructions;

iv. Adequate physical strength to attend cooking workshops.

Exclusion criteria

i. Without caregiver

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

136 participants in 2 patient groups

Assigned intervention
Other group
Description:
During the first 10 weeks, the intervention group will undergo the 10-week programme in the "Chef Anchor 3.0"
Treatment:
Other: 10-week programme
Assigned waitlist attention control
Other group
Description:
During the first 10 weeks, no activity for the waitlist control group. Then, from week 10 to 20, the waitlist control group will attend the same 10-week programme.
Treatment:
Other: 10-week programme

Trial contacts and locations

1

Loading...

Central trial contact

Pui Hing Chau, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems