NCT05949346

Brief Summary

The goal of this randomized controlled trial (RCT) is to develop and to implement a multiple family narrative therapy (MFNT) intervention consisting of parent-child relationships training among Chinese families of children with Dyslexia (CFCDs). The intervention aims to reduce the psychological distress of parents and their child, thus improving parent-child relationships, and the trial aims to assess the effectiveness of MFNT among them. A RCT design supplemented by qualitative interviews will be used to evaluate the effectiveness of MFNT on family welfare.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
123

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2022

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 6, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 6, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 9, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 18, 2023

Completed
Last Updated

July 18, 2023

Status Verified

March 1, 2021

Enrollment Period

1.3 years

First QC Date

July 9, 2023

Last Update Submit

July 9, 2023

Conditions

Keywords

DyslexiaNarrative therapyEfficacyInterventionMultiple family groupParent-childSpecial educational needs

Outcome Measures

Primary Outcomes (4)

  • Kessler Psychological Distress Scale (KPDS)

    Kessler Psychological Distress Scale is a 10-item scale completed by the child and the child's parent. It assesses the frequency of distress-related feelings in the past month on a 5-point Likert Scale (1=None of the time; 2=A little of the time; 3=Some of the time; 4=Most of the time; 5=All of the time). The scale is reliable and valid for the local context, given it will be delivered in Chinese. Changes in scores of Kessler Psychological Distress Scale will be evaluated before, after the intervention as well as at a follow-up assessment (3 months after the end of the intervention).

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

  • Parental Stress Scale (PSS)

    Parental Stress Scale (PSS) consists of 17 items on a 6-point scale (1 = strongly disagree; 2 = disagree; 3= somewhat disagree; 4 = somewhat agree; 5 = agree; 6 = strongly agree) measuring parents' perception of parental stress. Seven items require reverse scoring. A total score is calculated, with higher scores indicating higher levels of parental stress. The Chinese version of the scale has been translated and validated. Changes in its total score will be evaluated before, after the intervention as well as at a follow-up assessment (3 months after the end of the intervention).

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

  • Parent-Child Relationship Scale

    Parent-Child Relationship Scale is a scale that assesses subjects' perceptions of their current relationship with their children. It consists of 17 items based on 5-point scale, ranging from 1 = never to 5 = always. The scale uses mean score, and a higher score indicates a more positive parent-child relationship. Changes in its mean score will be evaluated before, after the intervention as well as at a follow-up assessment (3 months after the end of the intervention).

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

  • Parental Bonding Inventory (PBI)

    Parental Bonding Inventory (PBI) is a 25-item instrument assessing levels of parental care and overprotection perceived by the child. It consisted of two subscales termed 'care' and 'overprotection/control'. The measure is to be completed for both mothers and fathers separately, with each parent being scored on a 4-point Likert scale (Very unlike = 0, Moderately unlike = 1, Moderately like = 2, Very like = 3). Changes in the scores in "care" and "overprotection/control" subscales in both father and mother will be evaluated before, after the intervention as well as at a follow-up assessment (3 months after the end of the intervention).

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

Secondary Outcomes (2)

  • Satisfaction With Family Life Scale (SWFL)

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

  • Guilt and Shame Questionnaire (GSQ)

    1 week prior intervention, Intervention week 4, and 3 months post-intervention

Study Arms (2)

MFNT Intervention (Treatment Group)

EXPERIMENTAL

Parents of children with dyslexia who are randomized in Treatment Group will first take part in a pre-tested 4-session MFNT intervention programme. The parents will participate in lectures, group discussions, video demonstrations, and in-group exercises offered in these four mentored sessions, while their children will attend the second and fourth sessions.

Behavioral: Multiple Family Narrative Therapy (MFNT)

MFNT Intervention (Wait Listing Control Group)

EXPERIMENTAL

Families of children with dyslexia who are randomized in Wait Listing Control Group receive services as usual by the school personnel during the intervention period. The 4-session MFNT intervention program will be delivered to them after the intervention period.

Behavioral: School services for families of children with Dyslexia

Interventions

MFNT consist of 4 weekly group sessions with selected themes from both multiple family therapy (MFT) and narrative therapy (NT) offered in a group format. The family is treated as a system through both psychodynamic practices and attachment theories to manage symptoms, to achieve family resilience, and to empower both parents and child to share their unique and lived value-driven experiences. MFNT provides families with therapeutic environments that are conducive to learning and modelling in order to facilitate the process of building healthier parent-child dyads.

MFNT Intervention (Treatment Group)

Selected school personnel will deliver services as usual for the control group.

MFNT Intervention (Wait Listing Control Group)

Eligibility Criteria

Age7 Years - 13 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Participants 7-13 years old and their parents
  • Dyslexia diagnosis (by psychiatrist or educational psychologist or clinical psychologist)
  • Diagnosis with comorbidity of other learning disabilities
  • Cantonese speaking participants (child and parents)
  • At least one of the parents, but not siblings nor grandparents, can commit to all four sessions
  • Participants able to comply with all testing and study requirements

You may not qualify if:

  • Formal current diagnosis of psychosis
  • Limitation in daily communication
  • Previous service recipients of Narrative Therapy or Multiple Family Group
  • Non-Cantonese speaking child or parent
  • Parents or children who refuse to give written consent for their participation in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Social Work, Hong Kong Baptist University, Hong Kong, China

Hong Kong, Hong Kong

Location

MeSH Terms

Conditions

Dyslexia

Condition Hierarchy (Ancestors)

Language DisordersCommunication DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSpecific Learning DisorderLearning DisabilitiesSigns and SymptomsPathological Conditions, Signs and SymptomsNeurodevelopmental DisordersMental Disorders

Study Officials

  • Tak Mau Chan, PhD

    Hong Kong Baptist University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 9, 2023

First Posted

July 18, 2023

Study Start

January 1, 2022

Primary Completion

May 6, 2023

Study Completion

May 6, 2023

Last Updated

July 18, 2023

Record last verified: 2021-03

Locations