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EXercise Continuation Incorporating Technology Enhancements (EXCITE) Study

EXercise Continuation Incorporating Technology Enhancements (EXCITE) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02059382
Acronym
EXCITE
Enrollment
40
Registered
2014-02-11
Start date
2013-08-31
Completion date
2014-06-30
Last updated
2014-07-31

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

Conditions

Physical Inactivity

Keywords

daily physical activity, exercise, social support, online social network

Brief summary

The purpose of this study is to inform the integration of mobile and social media components into larger interventions aimed at increasing adherence and maintenance of physical activity. Nearly half of the US population do not meet physical activity recommendations of ≥150 minutes of moderate activity per week. The use of smartphones to self track data and upload that data to an online social network is becoming increasingly common and may be an effective way to motivate physical activity adherence and maintenance. We are proposing a two phase study to develop and evaluate a mobile health (mHealth) intervention that includes the use of two existing technologies: 1) the RunKeeper mobile app to collect and upload exercise data (distance, pace, time), and 2) the RunKeeper.com online social network as a place to analyze uploaded data and engage with a coach and online community. Phase 1 (n=10) will iteratively develop the mHealth intervention and phase 2 (n=30) will pilot the mHealth intervention (participants will be randomized to either mHealth intervention (n=20) or control (n=10)) to collect feasibility, acceptability and preliminary efficacy data. All participants will attend a day-long ChiWalk/Run training to help them avoid potential injuries and meet their coach and community in-person. All participants will also be asked to wear a FitBit accelerometer from one week before the beginning of the intervention through one week after the end of the intervention to collect total physical activity data. This data will be uploaded automatically to the study data base. Primary outcomes will be total physical activity as collected by the FitBit accelerometer (and the RunKeeper mobile app for the intervention group) and secondary outcomes will be changes in psychological factors that may mediate adherence to physical activity.

Interventions

BEHAVIORALChiRunning training
BEHAVIORALunblinded accelerometer
BEHAVIORALparticipation in online social network
BEHAVIORALparticipation in study website
BEHAVIORALTechnology support for behavior change

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy underactive adults interested in using mobile and web based technologies to increase their physical activity * low risk of cardiovascular disease * comfortable reading and communicating in English * owns a smartphone and is does not regularly use a fitness tracking mobile app * has regular access to the internet and a wireless connection for data uploading.

Exclusion criteria

* currently meeting/exceeding recommend 450 MET min per week * previous condition that would contraindicate regular moderate to vigorous physical activity

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of recruitmentEnd of 8 weeks of recruitmentMeeting 75% of recruitment goal of 40 participants
Feasibility of retentionEnd of 10 weeks of participationRetaining 75% of enrolled participants.
Feasibility for participant adherenceMeasured through out the 10 weeks of active participationWhether participants complete at least 75% of the exercise that they committed to at the beginning of the study.
Acceptability of study proceduresEnd of 10 weeks of active participationDid participants find study procedures acceptable?

Secondary

MeasureTime frameDescription
Change in body awarenessBaseline and end of 10 weeks of active participationWe used the Multi-dimensional Assessment of Interoceptive Awareness (MAIA) to measure body awareness. MAIA is a 32-item questionnaire with eight separately scored scales. .We used 3 of the 8 scales most relevant for an exercise intervention to assess body awareness. The subscales we used were: 1) Self-Regulation: ability to regulate distress by attention to body sensations; 2) Body Listening: active listening to the body for insight; 3) Trusting: experience of one's body as safe and trustworthy. Scales range from 0-5 with higher numbers representing higher aspects of body awareness with internal consistencies of α=0.83; 0.82; 0.79 on the Self-Regulation, Body Listening, and Trusting subscales, respectively.
Total number of new exercise related injuryMeasured through out the 10 weeks of active participationMeasure of pain or injury associated with structured exercise.
Change in social supportBaseline and end of 10 weeks of active participationWe will use the Social support and exercise survey (SSES) to assess social support. SSES is 26 item survey of social support for exercise available to the individual using separate (13 item) scales each for friends and for family.
Change in exercise self efficacyBaseline and end of 10 weeks of active participationWe will be using Multidimensional Self-Efficacy for Exercise Scale (MSES) to assess exercise related self efficacy. MSES is a 9-item instrument used to assess three dimension of exercise related self efficacy (task, scheduling and coping).
Average weekly physical activity in stepsMeasured through out the 10 weeks of active participationDaily step measured using a digital accelerometer.
Average weekly MET min of structured exerciseMeasured through out the 10 weeks of active participationAverage weekly metabolic equivalent of task (MET) minutes are a measure of time and intensity of physical activity.
Change in mindfulnessBaseline and end of 10 weeks of active participationWe will use the Five Factor Mindfulness Questionnaire (FFMQ) to assess changes in mindfulness. FFMQ is a 39-item questionnaire with five subscales (observing, describing, acting with awareness, non-judging of inner experience, and non-reactivity to inner experience) and a summary score ranging from 39 to 195. Internal consistencies range from α=0.75-0.91.

Countries

United States

Outcome results

None listed

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