Condition category
Nutritional, Metabolic, Endocrine
Date applied
15/02/2007
Date assigned
16/02/2007
Last edited
03/01/2012
Prospective/Retrospective
Retrospectively registered
Overall trial status
Completed
Recruitment status
No longer recruiting

Plain English Summary

Not provided at time of registration

Trial website

Contact information

Type

Scientific

Primary contact

Prof John Gregory

ORCID ID

Contact details

Department of Child Health
University Hospital of Wales
Heath Park
Cardiff
CF14 4XN
United Kingdom
+44 (0)29 20 747747
gregoryjw@cardiff.ac.uk

Additional identifiers

EudraCT number

ClinicalTrials.gov number

Protocol/serial number

HTA 03/46/09

Study information

Scientific title

Acronym

DEPICTED

Study hypothesis

The primary objective of the study is to determine whether a psychosocial intervention can improve clinical and psychological outcomes for children and teenagers experiencing diabetes. The intervention comprises a training programme for non-psychologist members of a paediatric diabetes team, incorporating the use of a patient agenda setting tool. The secondary objectives of the study are: 1) to evaluate the cost effectiveness of a psychosocial intervention for children and teenagers with diabetes; 2) to assess skill retention, competency and confidence of non-psychologist members of the paediatric diabetes team, in delivering the intervention.

More details can be found at http://www.hta.ac.uk/1450

Ethics approval

An application for ethical approval for the study (cluster-randomised multi-centre trial) has been submitted to the Thames Valley MREC. Decision pending (ref: 07/MRE12/9).

Study design

Cluster randomised trial of a psychosocial intervention for young people with diabetes involving 24 UK paediatric diabetes clinics.

Primary study design

Interventional

Secondary study design

Randomised controlled trial

Trial setting

Not specified

Trial type

Treatment

Patient information sheet

Condition

Paediatric diabetes (type 1)

Intervention

Please note that, as of 16 January 2008, the start and anticipated end date of this trial have been updated from 1 April 2007 and 31 December 2008 to 1 June 2005 and 31 March 2009, respectively.

Interventions:
The intervention under study comprises two components: an agenda-setting tool for patients and parents (consisting of a rigid folder and a pad of tear-off sheets) and training paediatric diabetes care clinicians to incorporate the tool into routine care, and to conduct conversations about behaviour change in relation to diabetes management. The agenda-setting tool will enable patients and parents to set the agenda for consultations and identify the topics they feel are most important in terms of disease management. Clinician training will enable the diabetes care team to talk about behaviour change and psychosocial issues related to management, and to guide patients and parents in using the tool.

Intervention type

Other

Phase

Not Specified

Drug names

Primary outcome measures

The primary outcome measure for patients is glycaemic control assessed using HbA1c at 1 year.

Secondary outcome measures

For diabetes care teams:
1. Competency in delivery of the psychosocial intervention immediately, 3 months and 1 year post training
2. Importance and confidence in conducting behaviour change discussions during consultations (before and after training and at 1 year)
3. Systemic service changes (including consultation times, and telephone/home contacts)

Clinical outcomes for patients at each clinic visit:
1. Height, weight, Body Mass Index (BMI)
2. Insulin type, dose and number of injections
3. Hypoglycaemic episodes

Psychosocial outcomes for patients at study entry and 1 year:
1. Diabetes-specific quality of life (Pediatric Quality of Life Inventory [PEDSQoL diabetes module]; Problem Areas in Diabetes [PAID: emotional impact]; global quality of life measure)
2. Diabetes self-care (items relating to mis-management)
3. Self-efficacy (perceived competency scale)
4. Patient enablement (coping)
5. Perceptions of diabetes care team (Health Care Climate Questionnaire [HCCQ]; items relating to communication between clinicians, feelings towards next visit, continuity of care)
6. Preferences for care (as measured by a Discrete Choice Experiment)

Psychosocial outcomes for parents/guardians at study entry and 1 year:
1. Parent quality of life/anxiety (Problem Areas in diabetes; global quality of life item)
2. Perceptions of diabetes team (HCCQ: items relating to communication between clinicians, feelings towards next visit, continuity of care)
3. Preferences for care (Discrete Choice Experiment)

Parent-completed proxy measures (for children aged 5-11):
1. Diabetes specific quality of life (PEDSQoL diabetes module; Problem Areas in Diabetes; global quality of life item)
2. Diabetes self care (mis-management)

Service use and cost outcomes:
1. Cost of intervention (including training)
2. Travel to clinic
3. School absences
4. Time off work (parent)
5. In-patient admissions (including Intensive Therapy Unit [ITU] and High Dependency Unit [HDU], particularly with ketoacidosis)
6. Accident and Emergency (A&E) attendances
7. Clinic attendances
8. Contacts with the diabetes team (home, telephone, electronic)
9. Other health service contacts (GP attendances, any other)
10. Medication/equipment use (insulin type & dose; testing strips; lancets; analysis strips; hypostop/glucogel/glucagon)

Overall trial start date

01/06/2005

Overall trial end date

31/03/2009

Reason abandoned

Eligibility

Participant 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.

Participant type

Patient

Age group

Child

Gender

Not Specified

Target number of participants

700 patients across 24 centres

Participant 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.

Recruitment start date

01/06/2005

Recruitment end date

31/03/2009

Locations

Countries of recruitment

United Kingdom

Trial participating centre

Department of Child Health
Cardiff
CF14 4XN
United Kingdom

Sponsor information

Organisation

Cardiff University (UK)

Sponsor details

-
Cardiff
CF10 3XQ
United Kingdom

Sponsor type

University/education

Website

http://www.cf.ac.uk/index.html

Funders

Funder type

Government

Funder name

NIHR Health Technology Assessment Programme - HTA (UK)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Results and Publications

Publication and dissemination plan

Not provided at time of registration

Intention to publish date

Participant level data

Not provided at time of registration

Results - basic reporting

Publication summary

1. 2010 protocol in http://www.ncbi.nlm.nih.gov/pubmed/20144218
2. 2011 results in http://www.ncbi.nlm.nih.gov/pubmed/21851764

Publication citations

  1. Protocol

    McNamara R, Robling M, Hood K, Bennert K, Channon S, Cohen D, Crowne E, Hambly H, Hawthorne K, Longo M, Lowes L, Playle R, Rollnick S, Gregory JW, Development and Evaluation of a Psychosocial Intervention for Children and Teenagers Experiencing Diabetes (DEPICTED): a protocol for a cluster randomised controlled trial of the effectiveness of a communication skills training programme for healthcare professionals working with young people with type 1 diabetes., BMC Health Serv Res, 2010, 10, 36, doi: 10.1186/1472-6963-10-36.

  2. Results

    Gregory J, Robling M, Bennert K, Channon S, Cohen D, Crowne E, Hambly H, Hawthorne K, Hood K, Longo M, Lowes L, McNamara R, Pickles T, Playle R, Rollnick S, Thomas-Jones E, Development and evaluation by a cluster randomised trial of a psychosocial intervention in children and teenagers experiencing diabetes: the DEPICTED study., Health Technol Assess, 2011, 15, 29, 1-202, doi: 10.3310/hta15290.

Additional files

Editorial Notes