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Effects of a Healthy Lifestyle Program on Health Outcomes in Older Adults

NCT03576209 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2021-01-20

No results posted yet for this study

Summary

Medical condition or disease under investigation : Quantitative and qualitative aspects of sleep, quality of life, functional ability and well-being in older adults (\>55years)

Purpose of clinical trial : To study the prospective effects of a healthy lifestyle program on quantitative and qualitative aspects of sleep, quality of life, functional ability and well-being in older adults.

Primary objective : Measure the effects of the intervention on quantitative and qualitative aspects of sleep

Secondary objective (s) : Measure the effects of the intervention on physical activity, quality of life, functional ability and well-being Social identity and leadership, social support and motivation

Trial Design : Intervention study : controlled before-and-after study

Sample Size : total sample size : 1.000 participants

Summary of eligibility criteria : Older adults aged above 55years

Included in intervention group : adults who are participating in the healthy lifestyle promotion program 'Lekker Actief', organized by OKRA

Included in control group : waitlist controls or controls (adults, members of OKRA, not participating in the health promotion program 'Lekker Actief')

Maximum duration of treatment of a subject :

* Start of Health promotion program 'Lekker Actief' : September 2018
* Measurements with accelerometers will start prior to the health promotion program 'Lekker Actief' : July 2018
* End of Health promotion program 'Lekker Actief' : December 2019
* Duration of Health promotion program 'Lekker Actief': 12 weeks
* Maximal duration : July 2018-December 2019

Conditions

  • Sleep
  • Quality of Life
  • Functional Ability
  • Well-being
  • Social Identity
  • Leadership
  • Social Support
  • Motivation

Interventions

BEHAVIORAL

healthy lifestyle program

Participants (intervention group) are following a 12 week health promotion program. They will count daily steps by pedometers and participate in weekly organised walks (within socio-cultural organisation)

Sponsors & Collaborators

  • KU Leuven

    lead OTHER

Principal Investigators

  • Julie Vanderlinden, phds · KU Leuven

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-03-01
Primary Completion
2020-01-31
Completion
2020-08-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03576209 on ClinicalTrials.gov