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Status unknownNCT04727203AHAAUpdated Jul 21, 2022

Active and Healthy Ageing for All: a Multi-component Healthy Lifestyle Program

An interventional study of AHAA in Health Promotion, sponsored by KU Leuven. Status unknown at 5 sites in Belgium. Open to participants aged 60 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-07-21.

Sponsored by KU Leuven · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Jul 2022), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Sep 2019, registered Jan 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
400
Allocation
Non-randomized
Ages
60 Years and older
Sex
All
01

Study summary

AHAA is a healthy lifestyle program offered to older adults aged 60+ years. The program is developed based upon co-creation with the target group and implemented and evaluated in several locations.

Read the detailed description
  1. co-creation : all participants will be questioned and included in the co-creation session
  2. implementation : the developed multicomponent healthy lifestyle program will be enrolled and implemented in 6 locations (community services for older adults in Flanders and Brussels)
  3. evaluation : the program will be evaluated (effects and process)
02

Conditions studied

  • Health Promotion

Keywords

  • ageing
  • healthy lifestyle
  • intervention
03

In context

Lead sponsor

KU Leuven is the lead sponsor of 371 studies on the registry; 63 are open to participants now.

Browse KU Leuven studies →

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • age 60+ years

Exclusion criteria

Exclusion Criteria:

  • not being able to attend the weekly meetings
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
400 participants (estimated)

Study arms

  • Experimental
    Intervention

    Partcipants in this group will receive the 8 week healthy lifestyle program

    Behavioral: AHAA

  • No intervention
    Control

    Participants in this group will not receive any intervention

Interventions

  • BehavioralAHAA

    Multi-component healthy lifestyle program

    Also known as: Active and healthy ageing for all

06

What researchers measure

Primary outcomes

  1. Physical activity measured by IPAQ

    Subjective physical activity

    Time frame: up to twelve weeks

  2. Physical activity measured by accelerometry

    Objective physical activity

    Time frame: up to twelve weeks

  3. Sedentary behaviour measured by accelerometry

    Objective sedentary behaviour

    Time frame: up to twelve weeks

  4. Sedentary behaviour measured by IPAQ

    Subjective sedentary behaviour

    Time frame: up to twelve weeks

  5. Nutrition questionnaire (self-reported)

    Nutrition

    Time frame: up to twelve weeks

  6. Sleep measured by accelerometry

    Objective sleep

    Time frame: up to twelve weeks

  7. Sleep measured by PSQI

    Subjective sleep

    Time frame: up to twelve weeks

Secondary outcomes

  1. well-being measured by WEMWBS

    well-being

    Time frame: up to twelve weeks

  2. Perceived stress measured by the perceived stress scale

    Perceived stress of participants

    Time frame: up to twelve weeks

  3. Perceived positive health status measured by a self-reported questionnaire

    Perceived positive health status

    Time frame: up to twelve weeks

  4. Health literacy measured by HLSQ self-reported questionnaire

    Health literacy

    Time frame: up to twelve weeks

  5. Social support measured by a self-reported questionnaire

    Social Support

    Time frame: up to twelve weeks

07

Study locations

5 of 5 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04727203
Lead sponsor
KU Leuven
Collaborators
Odisee University college for applied sciences
Responsible party
Julie Vanderlinden (Phdc, KU Leuven) — Principal investigator
First posted
Jan 27, 2021
Start date
Sep 1, 2019
Primary completion
Dec 31, 2023 (estimated)
Completion
Sep 30, 2024 (estimated)
Last update
Jul 21, 2022

Study contacts

Julie Vanderlinden, PHDc
Contact
julie.vanderlinden@odisee.be
003216321861
Julie Vanderlinden, PHDc
principal investigator · KU Leuven

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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