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Support for PARents of Children Living With ADHD - a Research Trial (SPARCLAR)

Primary Purpose

Attention Deficit Disorder With Hyperactivity

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Parents InC
Incredible Years
Sponsored by
University of Glasgow
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Attention Deficit Disorder With Hyperactivity focused on measuring Parenting support

Eligibility Criteria

5 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

• Parents of children aged 5-12 with a formal diagnosis of ADHD, following a standardised assessment from a paediatrician or a psychiatrist, referred to the Fife integrated ADHD pathway during the one year recruitment period will be eligible for inclusion.

Exclusion Criteria:

  • Families attending other parenting groups
  • Parents who have low proficiency in English (as this will compromise their ability to complete research measures or participate in a group intervention).
  • Participants already taking part in research on a parenting intervention will also be ineligible to participate.

Sites / Locations

  • NHS Fife Psychology DepartmentRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Parents InC

Incredible Years

Arm Description

Group parenting support intervention based around four pillars: 1) empowerment/ownership; 2) education on ADHD and its effect on family identity/ values; 3) positive parenting in the context of ADHD; 4) making sense of ADHD in a developmental context. It is delivered over 5 weekly 2-hour sessions, a 6 week break, and a follow-up session.

A group parenting support intervention aimed at strengthening parent-child interactions and attachment, reducing harsh discipline and fostering parents' ability to promote children's social, emotional, and academic development. The IY programme is delivered over 14 weekly 2-hour sessions. IY facilitators are videotaped during sessions to maintain intervention fidelity. IY also includes 1-4 pre-intervention preparation sessions which may involve home visits and telephone support and reminders.

Outcomes

Primary Outcome Measures

Number of parents willing to be randomised to Parents InC or Incredible Years.
Measured by number of parents agreed to randomisation throughout the study period.
Number of parents recruited and retained.
Measured by number of parents recruited and retained throughout the study period.
Research procedures feasibility and acceptability
Face to face interviews will be conducted with participating families to assess the feasibility and acceptability of research procedures.

Secondary Outcome Measures

Primary efficacy outcome: Parental Sense of Competence Scale.
17-items measure of parenting self-esteem questionnaire with 2 sub scales. Each item is rated on a 6 point Likert scale anchored by 1= "Strongly Disagree" and 6= "Strongly Agree". A higher score indicates a higher parenting sense of competency. There are no average scores or 'cut-off's' for this tool.
Eyberg Child Behaviour Inventory.
36-items measure (parent reported) that assesses the current frequency and severity of child's behaviour. Items are rated on a 7-point intensity scale and a yes/no Problem scale.
General Health Questionnaire.
12-items self-report measure of common psychiatric conditions of parents. Each item is accompanied with four responses; "Not at all", "No more than usual", "Rather more than usual" and "Much more than usual". Items are rated on a 4-point response scale.
ADHD Symptom Rating Scale-Version 1.
Self-report symptom checklist consisting of 18 DSM-IV criteria for parents. The checklist assesses occurrence frequency of each symptom.
Parenting Daily Hassles Scale.
18-items self-report measure of the frequency and intensity of 20 potential parenting 'hassles' to indicate parents stress. The items are rated on a frequency and intensity scale. The frequency scale is scored rarely =1, sometimes= 2, a lot= 3, and constantly = 4. The intensity scale is scored by adding the parents rating of 1-5 for each item. If a 0 has been scored for frequency on an item then it should be scored 0 for intensity. The range for this scale is 0 -100. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Goal Based Outcomes.
Taken from the Child Outcomes Research Consortium to identify goals and assess progression. Progress toward individual goal is rated on a scale from 0 (no progress) to 10 (goal has been reached). This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
EQ-5D-5L
Self-report measure of parent quality of life. The EQ-5D-5L is a descriptive system comprises 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, some problems, moderate problems, extreme problems. Parents will be also be asked to rate their health on a visual analogue scale. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Paediatric Quality of Life Inventory (PedsQL)
23-items questionnaire which covers 4 core dimensions (physical, social, emotional and school functioning). Each dimension has 4 levels: never = 0, almost never= 1, sometimes= 2, often= 3 and almost always= 4.
Strengths and Difficulties Questionnaire (SDQ)
25-items questionnaire which assesses child's emotional and behavioural problems. Each item is scored 0, 1 or 2. Somewhat true is always scored 1, but whether Not true and Certainly true are scored 0 or 2 depends on whether the item is framed as a strength or difficulty. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Participant service use
Measured using diaries

Full Information

First Posted
December 4, 2018
Last Updated
March 11, 2019
Sponsor
University of Glasgow
Collaborators
NHS Fife, Chief Scientist Office of the Scottish Government
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1. Study Identification

Unique Protocol Identification Number
NCT03832270
Brief Title
Support for PARents of Children Living With ADHD - a Research Trial
Acronym
SPARCLAR
Official Title
SPARCLAR: A Feasibility Randomised Controlled Trial of a Parenting Support Programme Focussed on Families Affected by ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 21, 2019 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
October 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Glasgow
Collaborators
NHS Fife, Chief Scientist Office of the Scottish Government

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Attention-Deficit/Hyperactivity Disorder (ADHD) is a chronic and pervasive disorder characterised by problems in attention, impulse control and activity regulation that substantially burdens patients, families, and society. The efficacy of behavioural training for parents of children with ADHD symptoms is well established, however it is less clear which type of parenting intervention should be offered, and which aspects of parenting behaviour to focus on. It is not established whether an intervention designed specifically for families of children with a diagnosis will be more effective and cost effective than less specifically-targeted interventions. The purpose of this study is to determine the feasibility and likely size of a substantive randomised controlled trial comparing an AHDH specific parenting intervention to a diagnostically less-specific parenting intervention.
Detailed Description
Attention-Deficit/Hyperactivity Disorder (ADHD) is a chronic and pervasive disorder characterised by problems in attention, impulse control and activity regulation that substantially burdens patients, families, and society. ADHD is often associated with challenging behaviours that can induce negativity, even in parents who would otherwise cope well.The efficacy of behavioural training for parents of children with ADHD symptoms is well established, however it is less clear which type of parenting intervention should be offered, and which aspects of parenting behaviour to focus on. It is not established whether an intervention designed specifically for families of children with a diagnosis will be more effective and cost effective than less specifically-targeted interventions. Parents In Control (Parents InC) offers specific support around empowerment, information and behaviour management specific to ADHD, as well as understanding of the child's development context. Parents InC has been used for a number of years in Scotland and has been evaluated, with promising results, but with relatively small sample sizes, no long-term follow-up, no economic evaluation and, most crucially, no comparison to an alternative intervention or to a control group. The investigators now need to understand if it: i) is at least as effective as the current best-evidenced alternative, Incredible Years, in impacting children's behaviour outcomes; ii) is cost-effective; and iii) offers something helpful and unique compared to other parenting programmes in terms of parenting self-competence and quality of life. The purpose of this study is to determine the feasibility and likely size of a substantive randomised controlled trial comparing an ADHD specific parenting intervention to a diagnostically less-specific parenting intervention (Incredible Years). Specific objectives are to test (1) whether parents of children recently diagnosed with ADHD are willing to be randomised to Parents InC or IY; (2) whether sufficient numbers of families can be (a) recruited and (b) retained such that a full-scale RCT is likely to be feasible; (3) whether research procedures and efficacy measures are feasible and acceptable to participating families (including health economic measures and consent to link to routine datasets); (4) whether families participating in Parents InC achieve similar scores on the parenting sense of competence scale at 12 months post randomisation as those in the comparison arm (Incredible Years); (5) Whether the two intervention arms significantly differ on any other measures; and (6) the mean cost per participant of Parents InC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Disorder With Hyperactivity
Keywords
Parenting support

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel pilot RCT (MRC feasibility phase)
Masking
ParticipantOutcomes Assessor
Masking Description
Participants and assessors will be blind to treatment allocation.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Parents InC
Arm Type
Experimental
Arm Description
Group parenting support intervention based around four pillars: 1) empowerment/ownership; 2) education on ADHD and its effect on family identity/ values; 3) positive parenting in the context of ADHD; 4) making sense of ADHD in a developmental context. It is delivered over 5 weekly 2-hour sessions, a 6 week break, and a follow-up session.
Arm Title
Incredible Years
Arm Type
Active Comparator
Arm Description
A group parenting support intervention aimed at strengthening parent-child interactions and attachment, reducing harsh discipline and fostering parents' ability to promote children's social, emotional, and academic development. The IY programme is delivered over 14 weekly 2-hour sessions. IY facilitators are videotaped during sessions to maintain intervention fidelity. IY also includes 1-4 pre-intervention preparation sessions which may involve home visits and telephone support and reminders.
Intervention Type
Behavioral
Intervention Name(s)
Parents InC
Intervention Description
Based on social learning theory, Parents InC has been designed specifically for parents of children with an ADHD diagnosis with a particular focus on parenting sense of self competence.
Intervention Type
Behavioral
Intervention Name(s)
Incredible Years
Intervention Description
Also based on social learning theory but focus is not specifically on ADHD.
Primary Outcome Measure Information:
Title
Number of parents willing to be randomised to Parents InC or Incredible Years.
Description
Measured by number of parents agreed to randomisation throughout the study period.
Time Frame
Continuous over 1 year study period
Title
Number of parents recruited and retained.
Description
Measured by number of parents recruited and retained throughout the study period.
Time Frame
Continuous over 1 year study period
Title
Research procedures feasibility and acceptability
Description
Face to face interviews will be conducted with participating families to assess the feasibility and acceptability of research procedures.
Time Frame
Continuous over 1 year study period
Secondary Outcome Measure Information:
Title
Primary efficacy outcome: Parental Sense of Competence Scale.
Description
17-items measure of parenting self-esteem questionnaire with 2 sub scales. Each item is rated on a 6 point Likert scale anchored by 1= "Strongly Disagree" and 6= "Strongly Agree". A higher score indicates a higher parenting sense of competency. There are no average scores or 'cut-off's' for this tool.
Time Frame
Baseline, 12-months post-randomisation
Title
Eyberg Child Behaviour Inventory.
Description
36-items measure (parent reported) that assesses the current frequency and severity of child's behaviour. Items are rated on a 7-point intensity scale and a yes/no Problem scale.
Time Frame
Baseline, 12-month post-randomisation
Title
General Health Questionnaire.
Description
12-items self-report measure of common psychiatric conditions of parents. Each item is accompanied with four responses; "Not at all", "No more than usual", "Rather more than usual" and "Much more than usual". Items are rated on a 4-point response scale.
Time Frame
Baseline, 12-month post-randomisation
Title
ADHD Symptom Rating Scale-Version 1.
Description
Self-report symptom checklist consisting of 18 DSM-IV criteria for parents. The checklist assesses occurrence frequency of each symptom.
Time Frame
Baseline, 12-month post-randomisation
Title
Parenting Daily Hassles Scale.
Description
18-items self-report measure of the frequency and intensity of 20 potential parenting 'hassles' to indicate parents stress. The items are rated on a frequency and intensity scale. The frequency scale is scored rarely =1, sometimes= 2, a lot= 3, and constantly = 4. The intensity scale is scored by adding the parents rating of 1-5 for each item. If a 0 has been scored for frequency on an item then it should be scored 0 for intensity. The range for this scale is 0 -100. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Time Frame
Baseline, 3 months post Baseline (if applicable), 12-month post-randomisation
Title
Goal Based Outcomes.
Description
Taken from the Child Outcomes Research Consortium to identify goals and assess progression. Progress toward individual goal is rated on a scale from 0 (no progress) to 10 (goal has been reached). This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Time Frame
Baseline, 3 months post Baseline (if applicable), 12-month post-randomisation
Title
EQ-5D-5L
Description
Self-report measure of parent quality of life. The EQ-5D-5L is a descriptive system comprises 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, some problems, moderate problems, extreme problems. Parents will be also be asked to rate their health on a visual analogue scale. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Time Frame
Baseline, 3 months post Baseline (if applicable), 12-month post-randomisation
Title
Paediatric Quality of Life Inventory (PedsQL)
Description
23-items questionnaire which covers 4 core dimensions (physical, social, emotional and school functioning). Each dimension has 4 levels: never = 0, almost never= 1, sometimes= 2, often= 3 and almost always= 4.
Time Frame
Baseline, 12-month post-randomisation
Title
Strengths and Difficulties Questionnaire (SDQ)
Description
25-items questionnaire which assesses child's emotional and behavioural problems. Each item is scored 0, 1 or 2. Somewhat true is always scored 1, but whether Not true and Certainly true are scored 0 or 2 depends on whether the item is framed as a strength or difficulty. This measure will be re-collected if there is > 3 months wait period between baseline data collection and the start date of the parenting groups. This will allow the investigators to detect any baseline measure changes over the wait period.
Time Frame
Baseline, 3 months post Baseline (if applicable), 12-month post-randomisation
Title
Participant service use
Description
Measured using diaries
Time Frame
12-month post-randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • Parents of children aged 5-12 with a formal diagnosis of ADHD, following a standardised assessment from a paediatrician or a psychiatrist, referred to the Fife integrated ADHD pathway during the one year recruitment period will be eligible for inclusion. Exclusion Criteria: Families attending other parenting groups Parents who have low proficiency in English (as this will compromise their ability to complete research measures or participate in a group intervention). Participants already taking part in research on a parenting intervention will also be ineligible to participate.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fiona Sim
Phone
01413308254
Email
sparclar@glasgow.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Fatene Abakar Ismail
Phone
01413308254
Email
sparclar@glasgow.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucy Thompson
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Helen Minnis
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
Facility Information:
Facility Name
NHS Fife Psychology Department
City
Dunfermline
State/Province
Scotland
ZIP/Postal Code
KY11 4UW
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hilary Maddox, Dr
Phone
01383565400
Email
hilarymaddox@nhs.net
First Name & Middle Initial & Last Name & Degree
Caroline Hollinsworth
Phone
01383 565400
Email
carolinehollinsworth@nhs.net

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
The PIs will manage access rights to the data set. We anticipate that anonymised trial data may be shared with other researchers to enable international prospective meta-analyses.

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Support for PARents of Children Living With ADHD - a Research Trial

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