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

Catholic University (KU) of Leuven

Status: Completed

Conditions: Motivation; Well-being; Quality of Life; Social Support; Social Identity; Functional Ability; Sleep; Leadership

Treatments: Behavioral: healthy lifestyle program

Study type: Interventional

Funder types: Other

Identifiers

NCT03576209

Lekker Actief

Details and patient eligibility

About

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

Full description

This trial will consist of 3 visits : Pretest and posttest.

• Pretest measurements (week 0)

  o Accelerometry : a subsample of participants form intervention and control groups (n=400) will be asked to wear an accelerometer (type GT3X) during 7 entire days prior to baseline measurements. (Timing : July 2018-July 2019)

  o Baseline measurements : during the start up moment of the program all participants from intervention and control groups will be asked : (Timing : July 2018-July 2019)

  • To fill out the self-reported questionnaire (survey) : the survey is composed of existing validated scales : IPAQ, PSQI, SF-12, WEMWBS, HAQ-DI. (references of validated scales are provided in the 'outcome measures' section)
  • To perform a walk test over 20 meters in order to determine the individual stride length
  • To perform a 6 minute walking test in order to self-report perceived exertion and physical fitness (by Borg Scale) and to determine the individual entry level of the program (entry levels vary between 1-12)
  • To wear the Pedometer (Omron® Walking Style one 2.0) on a daily basis and register the amount of daily steps in their personal registration forms

• Posttest measurements (week 12)

  • Accelerometry : a subsample of participants form intervention and control groups (n=400) will be asked to wear an accelerometer (type GT3X®) during 7 days prior to posttest measurements. (Timing : September 2018 - December 2019)
  • Posttest measurements : at the end of the program all participants will be asked :

(Timing : September 2018 - December 2019)

• To fill out the self-reported questionnaire (survey). In addition to the pretest questionnaire, the validated scales ILI, Mael and Ashford (1992) and BREQ-3 will be added and will be filled out only by participants of the intervention groups
• To perform a 6 minute walking test in order to self-report perceived exertion and physical fitness (by Borg Scale)
• To inform the investigators on the amount of daily steps (measured with pedometer type : Omron® Walking Style one 2.0) during the 12 week program o Focus groups : a subsample will be invited to take part in focus groups. During these focus groups, participants will be encouraged to discuss the program and possible effects in small groups (5 participants per group). A semi-structured interview guide will be used to guide the discussions.

Enrollment: 1,000 patients

Sex: All

Ages: 55+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

-aged 55+ years

Exclusion criteria

-Participants who are physically unable to participate in weekly meetings (PAR-Q : Physical activity readiness scale) (Thomas et al., 1992)

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,000 participants in 2 patient groups

Intervention Group

Active Comparator group

Description:

12 week intervention

Treatment:

Behavioral: healthy lifestyle program

Control Group

No Intervention group

Description:

No walking program