Skip to main content
OpenTrials
Completed

NCT Number: NCT05557071

Increasing Physical Activity Among Early Career Professionals: A Feasibility Trial of an Online Intervention

Physical activity promotion remains a public health priority and accessible and scalable interventions are needed. Early career professionals are at-risk for inactivity and therefore a critical target for physical activity promotion. An online delivery format made up of web-based lessons and podcasts meets accessibility needs for this time-pressed population and has strong potential for reach.

This study explores the feasibility of a theory-based intervention which accounts for action control, namely by leveraging the the Multi-Process Action Control framework (M-PAC) and targeting factors such as incidental affect (e.g., work-related stress) through emotion regulation strategies grounded in the principles of Acceptance and Commitment Therapy.

The primary objective of this study is to examine the feasibility and acceptability of a 6-week web-based physical activity behaviour change program for early career professionals. Primary outcomes include rates of recruitment, attention, adherence as well as study satisfaction and intervention acceptability. Secondary measures will include physical activity and emotion regulation. Additional measures will explore Multi-Process Action Control constructs, perceived stress, applied mindfulness, action and acceptance, and valued living.

Completed

Looking for future studies?

Notify Me

Key information

Age range

25 year–44 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Victoria

Victoria, British Columbia, V8P 5C2, Canada

About this study

BACKGROUND

Despite the well-established physical and psychological benefit of physical activity, much of the population is not meeting recommended guidelines. Critical life transitions have been linked to physical activity decline and it follows that targeting those in transition is prudent. Early career professionals are one such critical demographic. Given the stress, demands, and time constraints that come with shifting to the workforce, it can be difficult to follow through on physical activity intentions. As such, an intervention designed to incorporate intention translation, mitigate incidental affect, and foster emotion regulation is warranted. This study will examine the feasibility of an accessible online intervention. Qualitative analysis will assist with refining the intervention and the protocol. Progression criteria will be used to determine whether revisions should be considered before proceeding to a definitive randomized controlled trial.

TARGET POPULATION

Early career professionals, operationalized as adults aged 25-44 and working at a desk-based job.

DESIGN

An open parallel feasibility randomized controlled trial will compare an online intervention condition to a waitlist control condition. This study features a controlled baseline with a post-intervention (6 weeks) evaluative design with an embedded qualitative and quantitative process evaluation.

INTERVENTION

Participants will be randomized to 1) a waitlist control group and 2) and Online Platform Intervention group.

Condition one: Waitlist control group representing the comparator. The control group will complete the baseline and final questionnaires. Following study completion, this group has the option of gaining access to the online platform for their own benefit.

Condition two: Intervention group. Those in the intervention condition will gain access to the online platform after completing a baseline questionnaire. Participants will engage in a self-guided 6 week program made up of weekly lessons. A 'booster session' will be offered at 3 weeks to check in regarding progress and engagement. A follow-up survey will be completed at 6 weeks, post-intervention. Participants will be invited to complete a qualitative semi-structured exit interview following final questionnaire completion.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • English speaking adults, aged 25-44, living in Canada, currently employed at least part-time in a desk-based job, currently not meeting physical activity guidelines, no contraindications to safely increase physical activity, access to the internet and a device to support the e-health application
  • Report no contraindications to physical activity (based on the completion of the Physical Activity Readiness Questionnaire administered at screening)

Exclusion criteria

  • No internet access, unable to speak/read English, meeting physical activity guidelines, existing chronic medical condition making them at risk of injury or ill health from increased physical activity
  • No exclusion criteria for sex, gender, medications, race or religion will be applied.

Treatment and study plan

Digital Health Behaviour Change Platform

Behavioral

Participants will gain access to 6 weekly lessons.

A series of 6 weekly educational modules including information on psychosocial determinants of physical activity engagement, adherence and maintenance, as well as corresponding behaviour change techniques and a number of other tools and strategies, such as reflection activities, quizzes, and worksheets. Mini podcasts are available to supplement the concepts introduced in the modules. The content is tailored for early career professionals. There will be an emphasis on tactics (e.g., mindfulness, acceptance, emotion regulation) to assist with overcoming incidental affect.

Primary outcomes

  1. Recruitment rate (monthly)

    Time frame: 4 months (at study completion)

    Primary outcome related to trial feasibility

  2. Participant retention

    Time frame: 6 weeks

    Primary outcome related to trial feasibility

  3. Adherence and engagement

    Time frame: 6 Weeks

    Primary outcome related to trial feasibility

  4. Study satisfaction and acceptabiity

    Time frame: 6 Weeks

    Primary outcome related to trial acceptability

Secondary outcomes

  1. Self-reported physical activity

    Time frame: 6 weeks

    measured using the Godin Leisure-Time Exercise Questionnaire (GLTEQ)

  2. Emotion regulation

    Time frame: 6 weeks

    Adapted from DERS-16 (Bjureberg et al., 2016)

Other outcomes

  1. Multi-Process Action Control constructs

    Time frame: 6 weeks

    Exploratory outcomes and manipulation checks

  2. ACT Constructs

    Time frame: 6 weeks

    Exploratory outcomes and manipulation checks

  3. Applied Mindfulness

    Time frame: 6 weeks

    Exploratory outcomes and manipulation checks

Sponsors and collaborators

Lead sponsor

University of Victoria

Other

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 27, 2022
Registry last updated
Sep 1, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.