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Trial · NCT07898384

Registered outcomes22

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

ListOutcomeTime frameDescription
PrimaryRecruitment and withdrawal rates12 weeksRecruitment rates (more than 70%) and withdrawal rates (less than 15%) as calculated using data recorded in participant recruitment log.
PrimaryAdherence12 weeks
Adherence with iP2P/iParent2Parent program (more than 80% rate of completion of at least five audio or video calls over 12 weeks and 100% rate of completion of all online outcome measures) as calculated using data recorded in participant program tracking log.
PrimaryAcceptability/Level of engagement12 weeks
Acceptability and level of engagement of the iP2P/iParent2Parent program intervention as measured through focus groups/interviews with mentors and interviews with mentees guided by the Theoretical Framework of Acceptability. Focus groups and interviews will take approximately 45 minutes per timepoint.
PrimaryBarriers/Enablers12 weeksBarriers and enablers of the iP2P/iParent2Parent program intervention as measured through focus groups/interviews with mentors and interviews with mentees.
SecondaryPerceived social role satisfaction (young adult mentor outcome)12 weeksPerceived social role satisfaction measured by the PROMIS Satisfaction with Social Roles and Activities. Minimum value: 0 Maximum value: 100 Higher score indicates better outcome
SecondaryEmotional distress (young adult mentor outcome)12 weeksEmotional distress measured by the Generalized Anxiety Disorder-7 (GAD-7). Minimum value: 0 Maximum value: 21 Higher score indicates worse outcome
SecondaryEmotional distress (young adult mentor outcome)12 weeksEmotional distress measured by the Patient Health Questionnaire-8 (PHQ-8). Minimum value: 0 Maximum value: 24 Higher score indicates worse outcome
SecondaryPerceived social role satisfaction (parent mentor outcome)12 weeksPerceived social role satisfaction measured by the PROMIS Satisfaction with Social Roles and Activities. Minimum value: 0 Maximum value: 100 Higher score indicates better outcome
SecondaryEmotional distress (parent mentor outcome)12 weeksEmotional distress measured by the Generalized Anxiety Disorder-7 (GAD-7). Minimum value: 0 Maximum value: 21 Higher score indicates worse outcome
SecondaryEmotional distress (parent mentor outcome)12 weeksEmotional distress measured by the Patient Health Questionnaire-8 (PHQ-8). Minimum value: 0 Maximum value: 24 Higher score indicates worse outcome
SecondaryEmotional distress (parent mentor outcome)12 weeksEmotional distress measured by the Parental Stress Scale (PSS). Minimum value: 18 Maximum value: 90 Higher score indicates worse outcome
SecondaryTransition readiness (adolescent/young adult mentee outcome)12 and 24 weeksTransition readiness measured by the Transition Readiness Assessment Questionnaire (TRAQ). Minimum value: 20 Maximum value: 100 Higher score indicates better outcome
SecondaryPerceived social support (adolescent/young adult mentee outcome)12 and 24 weeksPerceived social support measured by the Multidimensional Scale of Perceived Social Support (MSPSS). Minimum value: 12 Maximum value: 84 Higher score indicates better outcome
SecondaryEmotional distress (adolescent/young adult mentee outcome)12 and 24 weeksEmotional distress measured by the Generalized Anxiety Disorder-7 (GAD-7). Minimum value: 0 Maximum value: 21 Higher score indicates worse outcome
SecondaryEmotional distress (adolescent/young adult mentee outcome)12 and 24 weeksEmotional distress measured by the Patient Health Questionnaire-8 (PHQ-8). Minimum value: 0 Maximum value: 24 Higher score indicates worse outcome
SecondaryMentor quality (adolescent/young adult mentee outcome)12 and 24 weeksMentor quality measured by the Mentor Behaviour Scale. Minimum value: 15 Maximum value: 75 Higher score indicates better outcome
SecondaryEmotional distress (parent mentee outcome)12 and 24 weeksEmotional distress measured by the Generalized Anxiety Disorder-7 (GAD-7). Minimum value: 0 Maximum value: 21 Higher score indicates worse outcome
SecondaryEmotional distress (parent mentee outcome)12 and 24 weeksEmotional distress measured by the Patient Health Questionnaire-8 (PHQ-8). Minimum value: 0 Maximum value: 24 Higher score indicates worse outcome
SecondaryEmotional distress (parent mentee outcome)12 and 24 weeksEmotional distress measured by the Parental Stress Scale (PSS). Minimum value: 18 Maximum value: 90 Higher score indicates worse outcome
SecondaryCoping (parent mentee outcome)12 and 24 weeksCoping as measured by the Coping Health Inventory for Parents (CHIP-16). Minimum value: 0 Maximum value: 48 Higher score indicates better outcome

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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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