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Young People With All Long-term Health ConditionsNTESNCT05867745

The National Transition Evaluation Study

An observational study of Young People With All Long-term Health Conditions, run by University of Surrey at 7 sites in United Kingdom.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This is a multi-centre study within England to evaluate whether the Burdett Trust National Transition Network and the implementation of the Model of Improvement for Transition has an impact on the experience of transitioning from child to adult services for young people, and their families. Read more about this study

Who is it for?
Ages 12 years and olderHealthy volunteers can take part
What is being tested?
Interview, Survey and Letter to a friend (autoethnography)
How many people
100 participants
Where
7 sitesUnited Kingdom
Study dates
21 Apr 2023to 31 May 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Young people and parents/carers from the eight case study sites for this project are eligible to participate. Dyads of young people and parents will be invited to participate. In cases where either the parent or young person does not wish to take part, the other can still participate. The Lead Nurse for Transition and RNAs are eligible to participate due to their direct role in implementing the National Transition Network and the Model of Improvement for Transition. Transition champions and key professionals from the eight case study sites for this project are eligible to participate.

Who may be able to join

  • Young people aged 12 to 25 years (upper age limit determined during the mapping and their parents/carers)
  • Young people with any long-term health condition(s) that will require transfer to adult health care services and their parents/carers
  • Young people who have already transferred to adult health care services within the last two years (at the point of recruitment) and their parents/carers
  • The Lead Nurse for Transition and Regional Nurse Advisors directly involved in implementation of National Transition Network and the Model of Improvement for Transition
  • Transition champions and key professionals involved in the young person's transition from child to adult services from the eight services/organisations which from the case study sites

Who cannot join

  • Young people and parents/carers who the clinical team caring for them consider it not appropriate to invite them to participate.

Trial locations and contacts

7 sites in 1 country.

Pippa Sipanoun, PhD contact

07944138828

p.sipanoun@surrey.ac.uk

7 sites in 1 country

United Kingdom7 sites, 3 recruiting
  • Derian House Children's Hospice

    Chorley, Lancashire

    Active, not recruiting
  • Darent Valley Hospitals; Dartford and Gravesham NHS Foundation Trust

    Dartford

    Active, not recruiting
  • Imperial College Healthcare NHS Trust

    London

    Dougal Hargreaves, dougal.hargreaves@nhs.net

    Not yet recruiting
  • Oxleas NHS Foundation Trust

    London

    Active, not recruiting
  • Nottinghamshire Healthcare NHS Foundation Trust

    Nottingham

    Michelle Hancock, michelle.hancock@nottshc.nhs.uk

    Recruiting
  • Oxford University Hospitals NHS Trust

    Oxford

    Active, not recruiting
  • Sheffield Children's NHS Foundation Trust

    Sheffield

    Priya Narula

    Recruiting

Other trials in United Kingdom

About this study

Official title: Evaluation of the Development of the Burdett National Transition Nursing Network

This is a multi-centre study within England to evaluate whether the Burdett Trust National Transition Network and the implementation of the Model of Improvement for Transition has an impact on the experience of transitioning from child to adult services for young people, and their families. A concurrent mixed methods design will be utilised with qualitative (interviews/case studies), and quantitative descriptive (surveys) data collected simultaneously over three phases. Participants will include young people, parents, and professionals involved in the young person's transition journey.

Read the detailed description

This study forms the evaluation aspect to a large transition-related innovation that is taking place across England (https://www.leedsth.nhs.uk/burdett-national-transition-nursing-network/).

It is important to formally evaluate this process. The study has been designed to determine whether the Burdett National Transition Network and implementation of the Model of Improvement for Transition has an impact on the experience of transitioning from child to adult services for young people, and their families. The research team at the University of Surrey will conduct a three-phased, mixed methods study to understand the experiences of all relevant stakeholders involved in the Network and the model's implementation and transition service users. The overall aim is to document new learning to ensure maximum reach of the model within a network of transition care, and improve the outcomes for young people transitioning to adult services.

STUDY DESIGN Our intention is to undertake a process evaluation using a case study approach. The investigators want to look at the change from before, during and after the Model of Improvement for Transition's implementation. The investigators plan to gather data at the start of the project about what happens now, and then what happens as the Model of Improvement for Transition evolves. The investigators will also gather information that is already routinely collected on an ongoing basis in each of the sites working with the RNAs, as part of the overall implementation project. This will be provided in summary form. As this is an evolving process, this may include but may not be limited to the:

  1. Number of Transition Lead roles for a whole organisation;
  2. Number of organisations working through Transition QI process;
  3. Number of organisations with transition contact;
  4. Number of organisations with an Executive Lead for transition;
  5. Number of Quality Improvement (QI) transition pathways completed;
  6. Number of health-based youth workers that are in post to support transition;
  7. Number of organisations with processes in place to use feedback from young people to support service improvement;
  8. Number of organisations with effective Transition governance processes in place e.g. transition board, steering group, organisational policy and reporting.

Two organisations or services per region (eight study sites in total) that is involved in the transition of young people to adult health services will be selected as case studies, giving eight case studies in total. To inform an unbiased selection of cases, a list of criteria will be described a priori by the project team, a consensus will be reached on the type, and context of the services to be included based on maximum variation, for example, geography and deprivation score, size of institution or service, ethnic diversity of the population, type of long-term health condition. The investigators aim to include populations that are under-researched such as: young people with complex needs, mental health problems, looked after children, young people receiving palliative care, and those for whom English is not their first language.

THEORETICAL FRAMEWORK

The 'On Your Own Feet Ahead' framework provides a focus for our study. The framework addresses eight key elements of good transitional care, divided into three core categories:

  1. interventions to improve the organisation of care;
  2. interventions to stimulate independence and self-management of young people, and
  3. collaboration with young people (and their families) and within the multidisciplinary team of professionals, working both in child and adult health care.

METHODS

It is well recognised that the most challenging aspect of changing practice is implementation and 'normalisation' of the 'intervention': therefore both qualitative (interviews) and quantitative descriptive (surveys) will have an important role to play in gathering contextual information from staff regarding how the Model of Improvement for Transition is both received and delivered. In order to understand the context and how the Model of Improvement for Transition is received and delivered our evaluation over three phases with repeated measures will include:

  • The National Lead Nurse (Interviews)
  • Regional Nurse Advisors (Interviews)
  • Transition champions the Regional Nurse Advisors work with in the Trusts and key professionals in the various networks (case studies; survey/interviews)
  • Young people and their parents/carers (case studies: survey/letter to a friend)

DATA ANALYSIS Survey data will be exported from Qualtrics to SPSS for analysis. Data stored within Qualtrics will be deleted upon study completion. Participants will be given a unique study ID. Only the study team will know the identity of the participants, necessary for the integration and synthesis of the survey and letter to a friend data or interview data. Survey data quality will be assessed for item/scale missingness at each time point and handled in accordance with scale guidelines (where available). Survey data will be analysed using descriptive statistics (e.g., means (standard deviations), medians (interquartile range) for continuous data, frequencies for categorical data) and presented by key group characteristics where appropriate (e.g., age group, gender etc) If appropriate, changes in the measurements over time will be tested with two-tailed, paired sample T-tests and Wilcoxon Matched Pair Signed Rank tests (Transition champion/key professionals), and repeated measures ANOVA (young people and parents) . Statistical significance will be considered at p ≤0.05 and as an exploratory study no adjustments will be made for multiple comparisons.

Interviews with the RNAs and Lead Nurse will be transcribed for analysis by a transcription company approved by the University of Surrey. The confidentiality agreement is provided with this application and can be found in clause 15 of the Transcription purchase order terms and conditions document. Any identifying information (e.g. names of people/hospitals) will be removed from the transcripts by the Researcher following transcription. The interviews will be analysed using thematic analysis.

The narratives in videos from the letter/email/video to a friend activity will be analysed using qualitative content analysis. The videos will not be transcribed. The research team will develop a proforma for the parents' videos and a separate one for young people's videos. Proformas will be developed by the researchers watching two videos each and coming together to discuss the elements of the video. These proformas will be used for analysis of subsequent videos.

Study data will be stored within SharePoint on the University of Surrey's password protected server. Any files containing participant details will be password protected. Data will only be accessible to the research team at the University of Surrey.

Being tested
Interview, Survey, Letter to a friend (autoethnography)
Keywords
young people, parents, transition into adult services, long-term health conditions

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • InterviewOther

    As previously specified

  • SurveyOther

    As previously specified

  • Letter to a friend (autoethnography)Other

    As previously specified

Study groups in NCT05867745
Study groupRoleWhat they receive
Lead nurse for Transition/Regional Nurse AdvisorsThe Lead Nurse and RNAs will be interviewed using telephone or online via Zoom. The interviews will be recorded using a Dictaphone rather than being saved via Zoom. Recordings will then be saved on the University's secure, password protected SharePoint for the study. Only the research team, and the designated transcriber, will have access to interview data. At the start of the project, interviews have been conducted in a PPI format to explore in depth the programme, expectations of how it should work and its implementation in order for the research team to devise the study. For the purposes of the research, interviews will be undertaken at one year, two years, and at the end of the programme to further explore implementation of the programme, including what works well, challenges encountered and their perceptions of the impact the programme has on families' experiences.
Receives: Other: Interview
Young peopleYoung people aged 12 to 25 years will be invited to participate. Young people will be asked to complete surveys at baseline, six months to one year and 18 months. Survey: Online surveys (Qualtrics) will be used to collect data from young people participating in the case studies. Young people will be asked to provide basic demographic details: age, gender, health condition, and type of service they attend (children's/young person's/adults') and length of time since transfer to adult services (if already transitioned). Letter/email/video to a friend: Young people will also be asked to write a 'letter/email to a friend' to describe their experiences. This will be completed online with the survey. They will be invited to write a letter/email or record a video about a recent clinic appointment/encounter with a health professional.
Receives: Other: Survey; Other: Letter to a friend (autoethnography)
ParentsCase study: Parents/carers will be invited to participate alongside young people. We will aim transition (including preparation, transfer and within adult services). Survey: Parents/carers of young people participating in the case study will be invited to complete an online survey (Qualtrics). Basic demographic details will be requested about the parent: age and gender; and their child: age, gender, health condition, and type of service they attend (children's/young person's/adults'), length of time since transfer to adult services (if already transitioned). Letter/email/video about their experiences: Parents will also be asked to complete a written task/video. They will be asked to describe their experiences relating to the shift in responsibility towards their child as the primary partner in their own healthcare, how their child is moving (or has moved) towards greater independence and competence in self-management.
Receives: Other: Survey; Other: Letter to a friend (autoethnography)
Transition champions/key professionalsTransition champions and key professionals in participating Trusts who are involved in the care of young people included in the case studies will be identified by the RNAs. We will aim to involve staff from various professional roles. They will be invited to complete an online survey (using Qualtrics) during the first year and one at the end of the second year, towards the end of the project. The surveys will explore their views on the implementation of the programme, experiences of building/making changes to a transition service, including what works well, challenges encountered and their perceptions of the impact the programme has on families' experiences. One professional from each case study site will be interviewed via Zoom/telephone to explore these aspects more in-depth at the same time points as the surveys. Ideally, we will aim to interview the same professionals at both time points. Data access and storage for will be the same as for the Lead Nurse/RNA interviews.
Receives: Other: Interview; Other: Survey

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To evaluate processes and outcomes, and to evaluate the reach of the Model of Improvement for Transition for young people transitioning from child into adult services, increases over time will be demonstrated in:

    The number of Transition Lead roles for a whole organisation

    Measured: 2.5 years

  2. The investigators expect to see an increase in:

    The number of organisations working through Transition QI process

    Measured: 2.5 years

  3. The investigators expect to see an increase in:

    The number of organisations with transition contact

    Measured: 2.5 years

  4. The investigators expect to see an increase in:

    The number of organisations with an Executive Lead for transition

    Measured: 2.5 years

  5. The investigators expect to see an increase in:

    The number of Quality Improvement (QI) transition pathways completed

    Measured: 2.5 years

  6. The investigators also expect to see an increase in:

    The number of health-based youth workers that are in post to support transition

    Measured: 2.5 years

  7. Lastly, The investigators also expect to see an increase in:

    The number of organisations with processes in place to use feedback from young people to support service improvement

    Measured: 2.5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 May 2023
  2. Study start21 Apr 2023
  3. Primary completion31 May 2024 (estimated)
  4. Study completion31 May 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Other
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05867745
Sponsor's protocol ID
SPON 2022 05 FHMS
Other IDs
313576
Acronym
NTES
Status last verified
May 2023
First submitted
28 Apr 2023
Last updated
22 May 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Undecided at present

Publications

  • Porter L, Gibson F, Aldiss S, Morgan S, Stanton A, Carney S, Farooq A, Barlow I, Sultan H, Sipanoun P. Bringing Young People, Health and Social Care Professionals, Transition Champions and Policymakers Together Through Hybrid Methods of Participation: Creating a Space for Shared Understanding of What Is Required to Improve Young People's Healthcare Transition. Health Expect. 2025 Feb;28(1):e70136. doi: 10.1111/hex.70136.

    PubMed 39888226
  • Sipanoun P, Aldiss S, Porter L, Morgan S, Powell E, Gibson F. Transition of young people from children's into adults' services: what works for whom and in what circumstances - protocol for a realist synthesis. BMJ Open. 2024 Jan 4;14(1):e076649. doi: 10.1136/bmjopen-2023-076649.

    PubMed 38176872

Questions about this trial

What is this clinical trial studying?

An observational study of Young People With All Long-term Health Conditions, run by University of Surrey at 7 sites in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 22 May 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Pippa Sipanoun, PhD (07944138828, p.sipanoun@surrey.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To evaluate processes and outcomes, and to evaluate the reach of the Model of Improvement for Transition for young people transitioning from child into adult services, increases over time will be demonstrated in: (time frame: 2.5 years). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05867745, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 May 2023.

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