Exercise Clinical Trial
Official title:
A Multi-component Physical Activity Intervention for Adolescent Girls: Feasibility Cluster Randomised Controlled Trial
Verified date | February 2021 |
Source | Liverpool John Moores University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A four-arm randomised pilot trial involving: 1. Physical activity programme only - live exercise sessions, social support, standardised text messages 2. Individual behaviour change support only - regular one-to-one video calls with an activity mentor 3. Combined - Physical activity provision and individual behaviour change support 4. Usual care control All groups will be provided with a menu of physical activities. Objectives. To conduct a RE-AIM evaluation of a 6-month multi-component PA intervention for adolescent girls, through investigating: - Who the intervention reaches, how representative they are for the population (Reach, Adoption) and who is most likely to benefit from the intervention (Reach); - The extent to which the intervention is delivered as intended (Implementation), and factors that affect this (Adoption); - Preliminary impact on participants' PA, sedentary behaviour, cardiovascular fitness and psychological wellbeing at 3, 6 and 12 months (Effectiveness, Maintenance); - The qualitatively examine the acceptability of the intervention for adolescent girls, and identify necessary refinements; - To gather data to inform a sample size calculation for a main trail
Status | Active, not recruiting |
Enrollment | 160 |
Est. completion date | September 2021 |
Est. primary completion date | September 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 13 Years to 16 Years |
Eligibility | Inclusion Criteria: - Female - 13-16 years - Living in the UK or Ireland - Would like support with becoming more physically active - Ability to participate in moderate intensity physical activity according to the Physical Activity Readiness Questionnaire Exclusion Criteria: - Have taken part in previous HERizon study - Currently doing more than 1 hour of exercise or sport every day. - Currently pregnant - Not having access to at least ONE of the following: a smartphone, home computer, or parent smartphone. |
Country | Name | City | State |
---|---|---|---|
Ireland | Dublin City University | Dublin | |
United Kingdom | Liverpool John Moores University | Liverpool | Merseyside |
United Kingdom | University of Liverpool | Liverpool |
Lead Sponsor | Collaborator |
---|---|
Liverpool John Moores University | Dublin City University, University of Liverpool |
Ireland, United Kingdom,
Cowley ES, Watson PM, Foweather L, Belton S, Mansfield C, Whitcomb-Khan G, Cacciatore I, Thompson A, Thijssen D, Wagenmakers AJM. Formative Evaluation of a Home-Based Physical Activity Intervention for Adolescent Girls-The HERizon Project: A Randomised Controlled Trial. Children (Basel). 2021 Jan 22;8(2). pii: 76. doi: 10.3390/children8020076. — View Citation
Cowley ES, Watson PM, Foweather L, Belton S, Thompson A, Thijssen D, Wagenmakers AJM. "Girls Aren't Meant to Exercise": Perceived Influences on Physical Activity among Adolescent Girls-The HERizon Project. Children (Basel). 2021 Jan 7;8(1). pii: E31. doi: 10.3390/children8010031. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Process Evaluation | Using a mixed methods approach, this study aims to conduct an evaluation of this physical activity intervention across five different domains (R-reach, E-effectiveness, A-adoption, I-implementation and M-maintenance). | week 0, week 12, week 24 | |
Primary | Change in objective physical activity levels | Participants objective PA will be monitored continuously (i.e. 24 h/day) over a nine-day period using an accelerometer (actigraph GT9x software). This device will be worn on their non-dominant wrist and uses the same validated MEMS sensor as the Actigraph GT3X+ model which has been validated (Hanggi et al., 2013) and used extensively with adolescents (Corder et al., 2016). Using the Actigraph, total daily PA, moderate-to-vigorous PA and sedentary time can be assessed. | Baseline to post-intervention (week 12) | |
Secondary | Aerobic capacity | Measured by the 20m shuttle run test which has been validated as an effective instrument for adolescent aerobic capacity (Boreham et al., 1990). Participants will require 20m space e.g. garden or green space. Using the Resistance Training for Teens mobile app, participants will be given written and visual instructions of how to set up and perform the test. Participants are required to run back and forth between two markers (20m distance) on the sound of a beep. The audio can be played through the app. | week 0, week 12, week 24 | |
Secondary | Upper body strength | Participants will do a push up test to the cadence of an audio recording. As above, written and visual instructions on how to set up and perform the test are provided on the app, as well as the audio file which sets the push up cadence. Should participants not be able to do a full push up (starting in high plank on hands and toes), they can lower onto their knees. It is important that the push up variation they choose is the same for baseline and post-intervention for fair comparison. No equipment is needed. | week 0, week 12, week 24 | |
Secondary | Strength/ Power | Participants will do a long jump to assess their strength/power. They will start from one marker and just as far as they can and mark where they land. They will use a measuring tape to record this distance. If they do not have a measuring tape they can use their feet to measure and do this again for the post-intervention assessment for consistency. Again, the Resistance Training for Teens app provides visual and written instructions on set up and how to perform. | week 0, week 12, week 24 | |
Secondary | Change in Physical Activity Motivation | measured by the 19-item Behavioural Regulation in Exercise Questionnaire (BREQ3) (Markland and Tobin, 2004) plus an additional five-items (Wilson et al., 2006). Using a 5 point Likert scale, the maximum score is 5 which indicates a high level of that particular sub-scale of motivation, e.g. intrinsic motivation rr amotivation. | week 0, week 12, week 24 | |
Secondary | Change in Body Appreciation | measured by the 10-item Body Appreciation Scale (Avalos et al., 2005). Using a 5-point Likert scale, the maximum score is 5 which indicates a high level of body appreciation. | week 0, week 12, week 24 | |
Secondary | Change in Physical Activity Competence | measured by the 4-item Perceived Competence Scale (Matsui & Muratas, 1997). Using a 7-point Likert scale, the maximum score is 7 which indicates a high level of competence towards physical activity. | week 0, week 12, week 24 | |
Secondary | Change in Self-esteeem | measured by the 12-item Adolescent Self-Esteem Questionnaire (Hafekost et al., 2017). Using a 5-point Likert scale, the maximum score is 5 which indicates a high level of self-esteem | week 0, week 12, week 24 | |
Secondary | Change in objective physical activity levels | Participants objective PA will be monitored continuously (i.e. 24 h/day) over a nine-day period using an accelerometer (actigraph GT9x software). This device will be worn on their non-dominant wrist and uses the same validated MEMS sensor as the Actigraph GT3X+ model which has been validated (Hanggi et al., 2013) and used extensively with adolescents (Corder et al., 2016). Using the Actigraph, total daily PA, moderate-to-vigorous PA and sedentary time can be assessed. | Baseline to follow-up (week 24) |
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