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

Sponsor
KU Leuven (Other)
Overall Status
Recruiting
CT.gov ID
NCT04727203
Collaborator
Odisee University college for applied sciences (Other)
400
5
2
61
80
1.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: AHAA
N/A

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)

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
There are 6 groups in this interventionThere are 6 groups in this intervention
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Active and Healthy Ageing for All: a Multi-component Healthy Lifestyle Program (AHAA)
Actual Study Start Date :
Sep 1, 2019
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

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

Behavioral: AHAA
Multi-component healthy lifestyle program
Other Names:
  • Active and healthy ageing for all
  • No Intervention: Control

    Participants in this group will not receive any intervention

    Outcome Measures

    Primary Outcome Measures

    1. Physical activity measured by IPAQ [up to twelve weeks]

      Subjective physical activity

    2. Physical activity measured by accelerometry [up to twelve weeks]

      Objective physical activity

    3. Sedentary behaviour measured by accelerometry [up to twelve weeks]

      Objective sedentary behaviour

    4. Sedentary behaviour measured by IPAQ [up to twelve weeks]

      Subjective sedentary behaviour

    5. Nutrition questionnaire (self-reported) [up to twelve weeks]

      Nutrition

    6. Sleep measured by accelerometry [up to twelve weeks]

      Objective sleep

    7. Sleep measured by PSQI [up to twelve weeks]

      Subjective sleep

    Secondary Outcome Measures

    1. well-being measured by WEMWBS [up to twelve weeks]

      well-being

    2. Perceived stress measured by the perceived stress scale [up to twelve weeks]

      Perceived stress of participants

    3. Perceived positive health status measured by a self-reported questionnaire [up to twelve weeks]

      Perceived positive health status

    4. Health literacy measured by HLSQ self-reported questionnaire [up to twelve weeks]

      Health literacy

    5. Social support measured by a self-reported questionnaire [up to twelve weeks]

      Social Support

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • age 60+ years
    Exclusion Criteria:
    • not being able to attend the weekly meetings

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 LDC Aalst Belgium 9300
    2 LDC Brussel Belgium 1000
    3 Regie Ouderenzorg Gent Belgium 9000
    4 LDC Mechelen Belgium 2800
    5 Triamant Sint-Truiden Belgium 2800

    Sponsors and Collaborators

    • KU Leuven
    • Odisee University college for applied sciences

    Investigators

    • Principal Investigator: Julie Vanderlinden, PHDc, KU Leuven

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Julie Vanderlinden, Phdc, KU Leuven
    ClinicalTrials.gov Identifier:
    NCT04727203
    Other Study ID Numbers:
    • AHAA
    First Posted:
    Jan 27, 2021
    Last Update Posted:
    Jul 21, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Julie Vanderlinden, Phdc, KU Leuven

    Study Results

    No Results Posted as of Jul 21, 2022