NCT05918926UnknownNot Applicable
Salaso Moving More: The Impact of Digitally Delivered Precision Exercise in Helping People to Move More
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Bangor University
- Enrollment
- 96
- Locations
- 1
- Primary Endpoint
- Habitual physical activity
Study Overview
Brief Summary
The main objective of this study is to examine the influence of the digital exercise prescription platform in increasing habitual physical activity in people on a weight management programme.
Detailed Description
Participants will be provided with individualised exercise training from exercise specialists. Participants will be recruited from the BCUHB NHS KindEating programme for people who have obesity (BMI of >30 kg/m2). Participants will be recruited remotely, via their KindEating dietitian. The assessments and exercise programme will be conducted remotely in the participants' own home.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Enrolled into the KindEating programme with BCUHB
- •≥ 18 years of age
- •Able to provide written informed consent
Exclusion Criteria
- •Any uncontrolled medical condition that is exacerbated by exercise
- •Unstable angina, unstable or acute heart failure, new or uncontrolled arrhythmias, resting or uncontrolled tachycardia, uncontrolled hypertension >180/100 (in either), symptomatic hypotension, febrile illness, acute uncontrolled psychiatric illness, other rapidly progressing terminal illness, uncontrolled diabetes >16.7mmol, patient's currently undergoing anti-biotic treatment for cellulitis, acute infections active foot ulceration
- •Inability to provide informed consent
Outcomes
Primary Outcomes
Habitual physical activity
Time Frame: Change between baseline and 3 months (post intervention)
Global Physical Activity Questionnaire
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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