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The Feasibility of an Active Lifestyle Programme in Patients Recovering From Colorectal Cancer

Feasibility of a Physical Activity Intervention Informed by Self-Determination Theory With Patients Recovering From Colorectal Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02751892
Acronym
MOVE
Enrollment
28
Registered
2016-04-26
Start date
2013-10-31
Completion date
2014-09-30
Last updated
2016-04-26

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

Conditions

Colorectal Cancer

Brief summary

Long-term maintenance of physical activity behaviour change post-intervention remains challenging. This study is investigating the feasibility of a behaviour change intervention based on Self-Determination Theory in people recovering from colorectal cancer and its effects on behaviour change 6 months post-intervention.

Detailed description

This study was a randomized controlled feasibility trial consisting of a 3-months active lifestyle intervention and a 3-months follow-up period. Participants were allocated to an active lifestyle programme (ALP) or the standard (SC) care group. ALP was offered 12 supervised exercise sessions over 3 months and six supportive behaviour change workshops. SC was encouraged to continue with their usual lifestyle. The intervention was informed by Self-Determination Theory. The supervised exercise sessions took place in small groups of maximum 7 participants and lasted approximately 1 hour. Exercise included aerobic and resistance exercises. The behaviour change workshops were delivered in a motivational interviewing style, also in small groups of maximum 7 participants. Participants were followed-up at 6 months. There was no contact with participants during the post-intervention and follow-up period.

Interventions

The intervention is an activity lifestyle programme to increase physical activity behaviour post-intervention and to facilitate behaviour change maintenance at 3 months post-intervention.

Sponsors

University of East Anglia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* a histologically confirmed diagnosis of colorectal cancer with Dukes stages A-C * completed cancer treatment within the last 24 months, * be able to understand spoken and written English * score of 80 or more on the Karnofsky Performance Status Scale

Exclusion criteria

* already meeting general PA guidelines of 150 min of moderate PA or 75 min of vigorous intensity PA per week, * recent myocardial infarction * uncontrolled hypertension * a pacemaker * or unstable angina.

Design outcomes

Primary

MeasureTime frame
Change in minutes spent in moderate and vigorous intensity physical activity measure with the International Physical Activity Questionnaire long version0, 3, 6 months

Secondary

MeasureTime frameDescription
Change in psychological needs satisfaction measured with the psychological needs satisfaction in exercise scale0, 3, 6 months
Change in quality of life measure with the Functional Assessment of Cancer Therapy general0, 3, 6 months
Change in quality of life measure with the Functional Assessment of Cancer Therapy-colorectal0, 3, 6 months
Change in fatigue with the Functional Assessment of Cancer Therapy - fatigue0, 3, 6 months
Change in intention to exercise0, 3, 6 monthsassessed with Intention to exercise scale
Change in barriers to exercise0, 3, 6 monthsassessed with Barriers to Exercise scale
Change in physical fitness0, 3, and 6 monthsassessed with the modified Bruce treadmill test
Change in behavioural regulation measure with the Behavioural Regulation in Exercise Questionnaire version 20, 3, 6 months
Change in upper body strength-upper arm strength0, 3, 6 monthsAssessed with biceps curl test
Change in lower body strength0, 3, 6 monthsAssessed with 30 sec sit-to-stand test
Changes in body composition (% body fat) assessed with bioelectrical impedance analysis0, 3, 6 months
Change in antropometric measures (waist circumference, hip circumference0, 3, 6 monthsWaist and hip circumference will be used to calculate the waist-to-hip ratio
Changes in anthropometric measures (height, weight, BMI)0, 3, 6 monthsBody weight and body height will be used to calculate BMI
Change in minutes spent in moderate and vigorous intensity physical activity with accelerometry0, 3, 6 months
Change in upper body strength-grip strength0, 3, 6 monthsAssessed with grip dynanometer

Outcome results

None listed

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