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临床试验/NCT06310681
NCT06310681已完成不适用

A Co-adapted Community-based Participatory Group Programme for Parents/Carers of Children With Complex Neurodisability (ENCOMPASS): A Pilot and Feasibility Study

City, University of London4 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2024年6月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
4
主要终点
Recruitment - percentage of eligible participants who consent to take part

研究概览

简要总结

The goal of this pilot feasibility study is to test a co-adapted community-based group programme ("Encompass") with parents/carers of children with complex neurodisability under 5 years of age in East London in the UK.

The main questions it aims to answer are:

  • Is it feasible and acceptable to carry out this newly co-adapted programme with two groups of parents/carers of children with complex neurodisability under the age of 5?
  • Is it feasible to carry out an evaluation of the above programme, which could then inform a protocol for larger scale evaluation?

The main activities for the parent/carer participants will include:

  • Attending ten "Encompass" parent/carer groups
  • Filling in questionnaires at the start and end of the groups
  • Attending an interview with the researcher to discuss their experiences

The groups will be facilitated by a healthcare professional and a parent with lived experience. They will also be interviewed about their experiences after the groups have been completed.

详细描述

Background

Parents/carers of children with complex neurodisability continue to lack appropriate family-centred care. "Encompass" is a community-based group programme that was co-adapted from "Baby Ubuntu" in Uganda. It is an example of a 'decolonised healthcare innovation' as it is a low-cost solution from a low-income country for use in a resource-constrained UK National Health Service (NHS).

Methods and analysis

The investigators will conduct a mixed methods pilot feasibility study to determine the feasibility and acceptability of delivering and evaluating "Encompass" with parents/carers of children under 5 years with complex neurodisability in the UK. The investigators aim to recruit 20 parents/carers of children from two NHS trusts in England serving urban areas where there is high social deprivation and ethnic diversity. Recruited parents/carers will attend the 10-modular, participatory group programme over a 6-month period. Groups will be facilitated by a trained allied health professional and an 'expert parent' with lived experience. The primary outcomes of interest are the feasibility of delivering and evaluating the programme (recruitment, retention rates, acceptability as perceived by the parents/carers, facilitators and wider key stakeholders), intervention fidelity and participant adherence. Results will be collectively assessed against traffic light criteria. Pre-, post- and follow-up data collection questionnaires will include the Family Empowerment Scale (FES), the Power Ladder Question, the Parent Patient Activation Measure (P-PAM), Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS), EuroQoL-5D-5-level (EQ-5D-5L) and parent/carer greatest needs and goals questionnaire. Post-intervention semi-structured interviews will be conducted with parents/carers, facilitators and key stakeholders within the NHS.

Discussion

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Parents and carers:
  • Inclusion Criteria:
  • Care for a child (<5 years) with a complex neurodisability*
  • Have received a diagnosis for their child, which has been disclosed to them, even this is a diagnosis such as SWAN (Syndrome Without A Name)
  • Reside in the boroughs of Newham or Tower Hamlets, East London
  • ≥18 years of age.

排除标准

  • Have a child with a developmental disability where there are no functional physical impairments as part of their complex needs. For example, children diagnosed with Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, intellectual impairments will be excluded unless they have a functional physical impairment with a neurological cause too.
  • Have a child with a progressive neurological condition such as Duchenne's Muscular Dystrophy.
  • Have a child with a structural physical impairment not caused by a neurological event or neurological difficulties. For example, children born with a limb difference or a child with hearing loss.
  • Do not have capacity to consent
  • Do not meet the inclusion criteria as specified above
  • There are no exclusions based on language, as interpreting/translating services will be offered.
  • Parent Facilitator:
  • Inclusion Criteria:
  • Parents/carer of children with complex neurodisability who are identified through other services as potentially being able to facilitate a group as an 'expert parent'
  • Prior experience in training or using participatory approaches - not essential
  • Exclusion Criteria:
  • Inability to read and speak English
  • Inability to commit to a 6-month period of work to the best of their knowledge
  • Healthcare Professional Facilitator:
  • Inclusion Criteria:
  • Therapists or healthcare professionals who work with children with disabilities and who are open to learning with families about their children.
  • Need to be registered with the Health and Care Professionals Council and should ideally have > 5 years post-graduate experience working with a paediatric population
  • Confident in working with children with complex neurodisability, such as cerebral palsy
  • Exclusion Criteria:
  • Inability to read and speak English
  • Inability to commit to a 6-month period of work to the best of their knowledge
  • Key Stakeholders:
  • Inclusion Criteria:
  • Staff from the NHS that are either involved in the delivery or commissioning of community child health care services in Newham or Tower Hamlets.
  • Examples include clinical managers, service leads or commissioners.
  • Exclusion Criteria:

研究组 & 干预措施

"Encompass" group programme

Experimental

干预措施: "Encompass" group programme (Behavioral)

结局指标

主要结局

Recruitment - percentage of eligible participants who consent to take part

时间窗: Before the groups commence, 3 months

Green light - 35% who are eligible consent to participate Amber light - 15-34% who are eligible consent to participate Red light - Less than 15% who are eligible consent to participate

Group Attendance

时间窗: End of each group, 6 months

Green light - More than 80% of parents/carers attend the group for 6+ sessions Amber light - 30-79% of parents/carers attend the group for 6+ sessions Red light - Fewer than 30% attend the group for 6+ sessions Feasibility, acceptability, and process outcome measures will be used. Quantitative data will be collected to assess the Traffic Light criteria. The green light signifies that criteria for progression has been met and a larger evaluation could proceed, the amber light suggests certain amendments need to be made and the red light indicates that the criteria for progression have not been met and researchers should not continue to a trial.

Fidelity - delivery on items described in the Fidelity Checklist

时间窗: End of each group, 6 months

Green light - 70% or greater score on the checklist Amber light - 50-69% score on the checklist Red light - Less than 50% score on the checklist

Follow-up response rate-self-complete outcomes questionnaire(s)

时间窗: Through the groups and 3 months post-groups, approximately 9 months

Green light - 70% or greater response to follow up Amber light - 50-69% response to follow up Red light - Less than 50% response to follow up

次要结局

  • Parent/carer Quality of Life - EuroQoL-5D-5-level (EQ-5D-5L)(First and final groups, 6 months)
  • Parent Patient Activation Measure (P-PAM)(First and final groups, 6 months)
  • Parent/carer Needs and Goals(First group, 1 month)
  • Childhood Cost Calculator (C3)(End of study, 9 months)
  • Family Empowerment Scale (FES)(First and final groups, 6 months)
  • Power Ladder Question (PLQ)(First and final groups, 6 months)
  • Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS)(First and final groups, 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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