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Trial · NCT06556719

Registered outcomes16

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryFeasibility of Intervention Measure (FIM)Measured at week 0 and week 6How feasible the intervention was from the perspective of the participants. This is measured through questionnaire.
PrimaryAcceptability of Intervention Measure (IAM)Measured at week 0 and week 6How acceptable the intervention is to the participants. This is measured through questionnaire.
PrimaryIntervention Appropriateness Measure (AIM)Measured at week 0 and week 6How appropriate the intervention is to the participants. This is measured through questionnaire.
SecondaryDaily Total Physical Activity of ParticipantsWeek 1 (for 7 days), and week 6 (for 7 days)Accelerometers (Axivity - AX3 model) will be used to track total daily physical activity
SecondaryHeart Rate of ParticipantsHR will be taken at week 0 and week 6 before and following the 6-minute walk test.heart rate measured via a blood pressure monitor
SecondaryBlood Pressure of ParticipantsBP will be taken at week 0 and week 6 before and following the 6-minute walk test.Blood pressure measured via a blood pressure monitor
SecondaryBasic Psychological Needs of Participants in Intervention EnvironmentAssessed at week 0 and week 6
Basic Psychological Needs and Satisfaction and Frustration scale. This entails feelings/perceptions of autonomy, relatedness, competence, enjoyment, satisfaction, and frustration in the study setting. Higher scores indicate greater satisfaction.
SecondaryPhysical Literacy of ParticipantsAssessed at week 0 and week 6the Canadian Assessment of Physical Literacy second addition (CAPL-2) will be used. A higher score on the CAPL-2 indicates higher physical literacy.
SecondaryCardiovascular Fitness Levels of ParticipantsAssessed at week 0 and week 6the 6-minute walk test will be used to assess changes in fitness. Greater distance walked in the 6 minute time frame is related to greater levels of cardiovascular fitness.
SecondaryMuscular Endurance Levels of ParticipantsAssessed at week 0 and week 6The plank test will be used to assess changes in fitness. The longer the plank is held, the greater the muscular endurance of the participant.
SecondaryDaily screen timeAssessed at week 0 and week 6
data from participants' phone settings will be used to capture daily screen time. Participants will navigate to their screen time settings, where a comprehensive and objective report of their weekly screen time (including average daily screen time) is available. Here, participants will screenshot this data and airdrop it to a secured IU dropbox location.
SecondaryDaily social media usageAssessed at week 0 and week 6
data from participants' phone settings will be used to capture daily screen time. Participants will navigate to their screen time settings, where a comprehensive and objective report of their weekly screen time (including average daily social media usage) is available. Here, participants will screenshot this data and airdrop it to a secured IU dropbox location.
SecondarySocial media addictionAssessed at week 0 and week 6participants will complete the Bergen Social Media Addiction Scale to assess social media addiction.
SecondaryInhibitory controlAssessed at week 0 and week 6The Color-Word trial from the Stroop Color and Word Test will be delivered on an iPad/tablet to participants to measure inhibitory control.
SecondaryBody SatisfactionAssessed at week 0 and week 6The Body Satisfaction Questionnaire (BSQ) will be completed to assess participants satisfaction of their body shape.
SecondaryBody AppreciationAssessed at week 0 and week 6The Body Appreciation Scale (version 2) (BAS-2) will be completed to assess participants' appreciation of their bodies.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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