The INTErGenerational intervention taRgeting fraIlTY trial (INTEGRITY)
- Conditions
- FrailtyPublic Health - Other public health
- Registration Number
- ACTRN12623000127606
- Lead Sponsor
- The George Institute for Global Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1100
Inclusion criteria for adults:
•aged 65 or over
•able to walk approximately 6m with or without a walking aid (self-reported)
•able to sit and stand from a chair with arms
•a baseline Telephone Montreal Cognitive Assessment score of 19 or more
•residing in the community (may be receiving aged care at home but not residing in residential aged care)
•Fully vaccinated against COVID or other current infectious disease in accordance with current guidelines at the time of the trial
•Written/digital informed consent
Inclusion criteria for children:
•aged 3-4
•attending the preschool at the study site or an affiliated preschool
•not attending school the next year
•fully toilet trained
•who have provided verbal assent
•where parents/guardians have provided written informed consent
•Fully vaccinated against COVID-19 or other current infectious disease in accordance with current requirements at the time of the trial
Inclusion criteria for educators:
•Be a qualified pre-school educator at one of the participating pre-schools
Key exclusion criteria for adults:
• has speech or sensory deficits that prevent interaction
• does not have an up to date/valid working with children check
Key exclusion criteria for children:
• has challenging behaviors that may affect their ability to participate in the program
Key exclusion criteria for educators:
• not familiar with the children who are participating in the research project
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in older adult frailty measured using the Frailty Index (FI)[ At baseline and post-intervention (after at least 17 weeks of the intervention)]
- Secondary Outcome Measures
Name Time Method