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Completed

NCT Number: NCT03554824

Psychosocial Outcomes and Transition Readiness in Uveitis

It is widely acknowledged that the transition from paediatric to adult health services should be a multidimensional and multidisciplinary process that addresses the medical, psychosocial, and educational needs of adolescents and young adults (AYA). Despite this, there is currently a scarcity of research examining the relationships between psychosocial factors (e.g., anxiety, social support) and transition readiness in AYA with uveitis. This study therefore aims to examine the relationships between psychosocial factors and transition readiness in pre-transfer adolescents and post-transfer young adults aged 10-25 years diagnosed with JIA at a single centre.

In total, 25 adolescents aged 10-16 years, together with a parent/guardian, will participate at Sheffield Children's Hospital and 10 young adults aged 16-25 years will participate at Sheffield Teaching Hospitals. Participants completed a battery of self-report questionnaire measuring psychosocial factors (anxiety/depression, social support, family functioning, health-related quality of life) and transition readiness (transition knowledge and skills, self-efficacy). Uveitis disease severity was also measured during clinic appointments. A subset of participants will also be asked to take part in a focus group. This study received full ethical approval, and all participants will give their written informed assent or consent before taking part.

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Key information

Age range

10 year–25 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Sheffield Children's NHS Foundation Trust

Sheffield, United Kingdom

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of uveitis
  • Uveitis managed by either Sheffield Children's NHS Foundation Trust or Sheffield Teaching Hospitals NHS Foundation Trust
  • Fluent in English

Exclusion criteria

  • No diagnosis of uveitis
  • Uveitis not managed by either Sheffield Children's NHS Foundation Trust or Sheffield Teaching Hospitals NHS Foundation Trust
  • Not fluent in English

Treatment and study plan

Primary outcomes

  1. Generalised Anxiety

    Time frame: Day 1, when participants complete the study questionnaire

    Generalised Anxiety Disorder-7 Questionnaire (Spitzer et al., 2006)

Secondary outcomes

  1. Depression

    Time frame: Day 1, when participants complete the study questionnaire

    Patient Health Questionnaire-9 (Spitzer et al., 1999)

  2. Health-related quality of life

    Time frame: Day 1, when participants complete the study questionnaire

    Paediatric Quality of Life Generic Module (Varni et al., 2002)

  3. Social support

    Time frame: Day 1, when participants complete the study questionnaire

    Bath Adolescent Pain Questionnaire Social Support Subscale (Eccleston et al., 2005)

  4. Family functioning

    Time frame: Day 1, when participants complete the study questionnaire

    Bath Adolescent Pain Questionnaire Family Functioning Subscale (Eccleston et al., 2005)

  5. Prosocial and problem behaviours

    Time frame: Day 1, when participants complete the study questionnaire

    Strengths and Difficulties Questionnaire (Goodman, 1997)

  6. Uveitis disease severity

    Time frame: Day 1, during hospital clinic appointment

    Standardization of uveitis nomenclature (SUN) scores will be used to assess uveitis disease severity.

Sponsors and collaborators

Lead sponsor

Sheffield Children's NHS Foundation Trust

Other

Collaborators

  • Sheffield Teaching Hospitals NHS Foundation Trust

Registry information

Official study title

Describing Relationships Between Psychosocial Outcomes and Readiness for Transition in Adolescent and Young Adult Patients With Uveitis - a Pilot Study

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jun 13, 2018
Registry last updated
Sep 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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