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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05557071
Enrollment
28
Registered
2022-09-27
Start date
2022-02-18
Completion date
2023-06-30
Last updated
2023-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Promotion, Physical Activity

Keywords

Emotion Regulation, Intention-behaviour Gap, Early Career Professionals

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALDigital Health Behaviour Change Platform

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.

Sponsors

University of Victoria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 44 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Participant retention6 weeksPrimary outcome related to trial feasibility
Recruitment rate (monthly)4 months (at study completion)Primary outcome related to trial feasibility
Adherence and engagement6 WeeksPrimary outcome related to trial feasibility
Study satisfaction and acceptabiity6 WeeksPrimary outcome related to trial acceptability

Secondary

MeasureTime frameDescription
Emotion regulation6 weeksAdapted from DERS-16 (Bjureberg et al., 2016)
Self-reported physical activity6 weeksmeasured using the Godin Leisure-Time Exercise Questionnaire (GLTEQ)

Other

MeasureTime frameDescription
Multi-Process Action Control constructs6 weeksExploratory outcomes and manipulation checks
Applied Mindfulness6 weeksExploratory outcomes and manipulation checks
ACT Constructs6 weeksExploratory outcomes and manipulation checks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026