The 5R Shared Leadership Program in Older Adult Walking Groups

September 8, 2021 updated by: Katrien Fransen, KU Leuven

The 5R Shared Leadership Program in Older Adult Walking Groups: A Clustered Randomised Controlled Trial

To test the efficacy of the 5R Shared Leadership program in older adults on participants' identification with their walking group, group cohesion, walking activity, and well-being, compared to a regular group walking program, the investigators conducted a cluster randomised trial.

Study Overview

Detailed Description

All walking groups participated in a 12-week structured group walking program. Half of these walking groups were randomly assigned to the intervention condition and received additionally the 5R Shared Leadership Program

Study Type

Interventional

Enrollment (Actual)

503

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Vlaams-Brabant
      • Leuven, Vlaams-Brabant, Belgium, 3000
        • KU Leuven

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

55 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Being part of a community-based OKRA SPORT+ meeting point that engages in the 12-week walking program

Exclusion Criteria:

  • n/a

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: A structured 12-week group walking program
Participants engaged in an evidence-based 12-week walking program.
Participants engaged in an evidence-based 12-week structured walking program, which aimed to enhance participants' physical activity and aerobic fitness levels based on personalised walking schedules and weekly group walks organised by the community-based meeting points.
Experimental: A structured 12-week group walking program + 5RS
In addition to the 12-week group walking program, participants engaged in the 5R Shared Leadership Program, which implements a structure of shared leadership and strengthens the identity leadership skills of the appointed peer leaders.
Participants engaged in an evidence-based 12-week structured walking program, which aimed to enhance participants' physical activity and aerobic fitness levels based on personalised walking schedules and weekly group walks organised by the community-based meeting points.

The manualised 5RS program aims to develop the leadership qualities of peer leaders by teaching them how to create, embody, advance, and embed a collective sense of 'us' in their teams. More specifically, 5RS consists of two key components that involve (1) implementing a structure of shared leadership, and (2) strengthening the identity leadership skills of the appointed peer leaders (Fransen et al., 2020).

Fransen, K., Haslam, S. A., Steffens, N. K., Mallett, C. J., Peters, K., Mertens, N., & Boen, F. (2020). All for us and us for all: Introducing the 5R Shared Leadership Program. Psychology of Sport and Exercise, 51, 101762. https://doi.org/10.1016/j.psychsport.2020.101762 Haslam, S. A., Steffens, N. K., Peters, K., Boyce, R. A., Mallett, C. J., & Fransen, K. (2017). A social identity approach to leadership development: The 5R program. Journal of Personnel Psychology, 16(3), 113-124. https://doi.org/10.1027/1866-5888/a000176

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Identity leadership
Time Frame: 12 weeks
4-item Identity Leadership Inventory-Short Form
12 weeks
Group identification scale
Time Frame: 12 weeks

To assess participants' identification with their walking group, the investigators use the 4-item group identification measure (e.g., "I am glad to be a member of this walking group."), as suggested by Doosje et al. (1995). The cognitive, evaluative, and affective aspects of identification are evaluated on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).

Doosje B, Ellemers N, Spears R. Perceived intragroup variability as a function of group status and identification. J Exp Soc Psychol. 1995;31(5):410-36.

12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Group cohesion
Time Frame: 12 weeks
Group Environment Questionnaire - A higher score corresponds with a higher group cohesion
12 weeks
Well-being
Time Frame: 12 weeks
Warwick-Edinburgh Mental Well-Being Scale. It comprises 14 positively phrased items (e.g., "I've been feeling good about myself") rated on a 5-point Likert scale ranging from 1 (none of the time) to 5 (all of the time). A higher score corresponds with a higher well-being
12 weeks
Walking activity
Time Frame: 12 weeks
International Physical Activity Questionnaire - Short Form
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Katrien Fransen, PhD, KU Leuven

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2018

Primary Completion (Actual)

January 31, 2020

Study Completion (Actual)

August 31, 2020

Study Registration Dates

First Submitted

August 27, 2021

First Submitted That Met QC Criteria

September 3, 2021

First Posted (Actual)

September 9, 2021

Study Record Updates

Last Update Posted (Actual)

September 16, 2021

Last Update Submitted That Met QC Criteria

September 8, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The anonymised data will be shared upon publication.

IPD Sharing Time Frame

Upon publication

IPD Sharing Access Criteria

The data will be shared together with the article following the journal recommendations.

IPD Sharing Supporting Information Type

  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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