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A Sedentary Behaviour Reduction Intervention for People With COPD

Get Up For Your Health: A Behaviour Change Intervention to Reduce Sedentary Behaviour for People With COPD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04004585
Enrollment
21
Registered
2019-07-02
Start date
2019-06-19
Completion date
2019-12-18
Last updated
2020-06-04

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

Conditions

COPD

Keywords

Sedentary behaviour, Behaviour change, Theoretical Domains Framework

Brief summary

Chronic obstructive pulmonary disease (COPD) is a major cause of disability. Individuals with COPD are more likely to spend prolonged periods of time in sedentary behaviour (SB) and less in light physical activity compared to their healthy peers. SB is associated with exercise intolerance, reduced motivation to exercise, lower self-efficacy and more frequent acute exacerbations among people with COPD. To date, there is very limited information regarding behavioural approaches to reduce SB in people with COPD. The aim of this study is to examine the feasibility of a new 4-week theory-informed behaviour change intervention to reduce SB in individuals with COPD.

Interventions

BEHAVIORALGet Up For Your Health

The intervention is a 4-week behaviour change intervention underpinned by the Theoretical Domains Framework (TDF) that aims to reduce sedentary behaviour. The intervention consists of one individualized face-to-face session and 3 subsequent weekly points of contact (face-to-face meetings or phone calls). Behaviour change techniques will be provided including education, verbal persuasion, environmental restructuring and goal-setting.

Sponsors

West Park Healthcare Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* A diagnosis of COPD confirmed by spirometry Forced expired volume to forced vital capacity ration (FEV1/FVC) less than 0.7 * An ability to ambulate. * An ability to provide informed consent.

Exclusion criteria

* Presence of co-existing conditions that may prevent participation in the intervention.

Design outcomes

Primary

MeasureTime frameDescription
Enrollment rate4 weeksEnrollment rate is calculated as a percentage (number of people enrolled/ number of people approached)
Completion rate4 weeksPercentage of those enrolled who completed the program
Participants satisfaction4 weeksParticipant satisfaction will be assessed on a percentage scale of 0 to 100, with 100 being the best possible score.
Adherence to wearing the activity monitor4 weeksPercentage of those who were able to provide data for at least 8 hours per day of wearing time during waking hours and for at least 4 days/week for the entire duration of the study

Secondary

MeasureTime frameDescription
Change in outcome expectationsBaseline - week 4 (post-intervention)To assess the change in the outcome expectations using a 15-item scale adapted from the Multidimensional Outcome Expectations for Exercise Scale over time from baseline to post-intervention. The questionnaire is a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree), that assesses physical outcome expectations (6 items), social outcome expectations (4 items), and self-evaluative outcome expectations (5 items) with the higher the scores the more positive the outcome expectations are. The total score is the sum of the score of the 15 items.
Change in sedentary timeBaseline - week 4 (post-intervention)To assess the change in sedentary time as measured using an accelerometer from baseline to post-intervention.
Change in knowledge of sedentary behaviourBaseline - week 4 (post-intervention)To assess the change in sedentary behaviour using an 8-item True or False questionnaire with higher scores indicating better knowledge of sedentary behaviour
Change in number of sit-to-stand transitionsBaseline - week 4 (post-intervention)To assess the change in the number of sit-to-stand transitions as measured using an accelerometer from baseline to post-intervention.
Change in daily number of stepsBaseline - week 4 (post-intervention)To assess the change in the number of steps as measured using an accelerometer from baseline to post-intervention.
Change in self-efficacyBaseline - week 4 (post-intervention)To assess the change in self-efficacy to sit less using a scale adapted from the Multidimensional Self-Efficacy Scale over time from baseline to post-intervention. The scale consists of 9 items that measures 3 components of self-efficacy (task, coping and scheduling) with each item is measured on a scale of 0 (no confidence at all) up to 100 (complete confidence). The total score is the average of the scores of the 9 items.

Countries

Canada

Outcome results

None listed

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