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Clinical Trials/ISRCTN61568050
ISRCTN61568050
Completed
未知

Development and Evaluation of a Psychosocial Intervention for Children and Teenagers Experiencing Diabetes

Cardiff University (UK)0 sites700 target enrollmentFebruary 16, 2007

Overview

Phase
未知
Intervention
Not specified
Conditions
Paediatric diabetes (type 1)
Sponsor
Cardiff University (UK)
Enrollment
700
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Registry
who.int
Start Date
February 16, 2007
End Date
March 31, 2009
Last Updated
8 years ago
Study Type
Interventional

Investigators

Sponsor
Cardiff University (UK)

Eligibility Criteria

Inclusion Criteria

  • For teams/clinics:
  • Teams include a paediatrician with an interest in diabetes and a diabetes specialist nurse
  • For patients:
  • 1\. Type 1 diabetes
  • 2\. Aged 4\-15
  • 3\. Under care of diabetes team for duration of trial
  • 4\. Diagnosed more than 1 year ago
  • 5\. Parental/guardian and child consent (or assent where appropriate) given
  • 6\. ability of patient and at least one parent/guardian to complete study materials (questionnaires)
  • Children aged 4\-15 will be included to reflect as broad a range of patients as possible. Young people aged 16\+ may be in transition between paediatric and adult services at some point during the trial and are therefore excluded. Data collected from questionnaires is crucial to determining the effectiveness of the intervention. However, questionnaires are only available in English, as measures included have not been validated in other languages: this would be beyond the scope of the current study.; For teams/clinics:

Exclusion Criteria

  • For teams/clinics:
  • \<40 potentially eligible children/adolescents (diagnosed more than 1 year ago) attending the clinic
  • For patients:
  • 1\. Not under care of parent or guardian (i.e. a looked after child)
  • 2\. Co\-morbid chronic illness likely to impact on HbA1c independent of patient's ability to manage their diabetes (e.g. condition requiring steroid treatment, cystic fibrosis, renal failure)
  • 3\. In receipt of ongoing psychiatric/psychological therapy at the start of the study
  • 4\. Other patients judged by their clinical carer to be vulnerable due to existing medical or social condition
  • Criteria have been designed in order to be as inclusive as possible. Clinics with less than 40 patients will be excluded due to practicalities of recruiting sufficient patient numbers (30 per clinic) and fewer than 40 patients is not felt to constitute an adequate size for a specialist children's service. It is unfortunately not feasible to recruit children under a care order, due to the practical difficulties of obtaining appropriate consent: this is felt to be outside the scope of the current study. However, patients attending clinics where health professionals have undergone training are likely to benefit from increased awareness of psychosocial issues.; For teams/clinics:
  • \<40 potentially eligible children/adolescents (diagnosed more than 1 year ago) attending the clinic
  • For patients:

Outcomes

Primary Outcomes

Not specified

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