Neuro-psychosocial Teleassistance for Neuromuscular Diseases

Sponsor
University of Deusto (Other)
Overall Status
Completed
CT.gov ID
NCT06031701
Collaborator
(none)
40
1
2
19.9
2

Study Details

Study Description

Brief Summary

This is a clinical trial to assess the effect of a neuropsychosocial intervention by means of telecare aimed at children and adolescents aged 7-16 years with neuromuscular diseases. The intervention is carried out in groups of 5 participants and is organised in 12 sessions: 1 session per week of 1h duration. The intervention is aimed at strengthening aspects of social cognition, self-esteem, social skills and aims at a reduction of symptomatology and a general improvement of psychological well-being.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Neuro-psychosocial teleassistance program
N/A

Detailed Description

Development of a neuro-psychosocial tele-assistance programme for groups of children and adolescents affected by various neuromuscular diseases, including Duchenne/Becker muscular dystrophy, limb-girdle dystrophy, etc. In this project the variables of interest and intervention include social cognition, quality of life, psychological symptomatology and coping strategies. The aim of this study is to test whether this programme improves the indicators in the mentioned variables.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Quasi-experimental pretest-posttest design with a non-equivalent wait list control groupQuasi-experimental pretest-posttest design with a non-equivalent wait list control group
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of a Neuro-psychosocial Teleassistance Programme for Children With Neuromuscular Diseases
Actual Study Start Date :
Nov 2, 2021
Actual Primary Completion Date :
Nov 30, 2022
Actual Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Neuro-psychosocial intervention with 12 grupal sessions is offered

Behavioral: Neuro-psychosocial teleassistance program
The intervention is carried out in groups of 5 participants and is organised in 12 sessions: 1 session per week of 1h duration. The intervention is aimed at strengthening aspects of social cognition, self-esteem, social skills and aims at a reduction of symptomatology and a general improvement of psychological well-being.

Experimental: Control

Waiting list control group

Behavioral: Neuro-psychosocial teleassistance program
The intervention is carried out in groups of 5 participants and is organised in 12 sessions: 1 session per week of 1h duration. The intervention is aimed at strengthening aspects of social cognition, self-esteem, social skills and aims at a reduction of symptomatology and a general improvement of psychological well-being.

Outcome Measures

Primary Outcome Measures

  1. Social cognition - Emotion Recognition [3 months after the intervention]

    Affect Recognition subtest of the Social Perception Domain of the NEPSY-II in the Spanish edition (Korkman et al., 2014) measures the capacity to identify emotions (happy, sad, neutral, afraid, irrationally angry, and disgust) in various images of children

  2. Social cognition - Theory of mind - NEPSY-II [3 months after the intervention]

    Theory of Mind subtest of the Social Perception Domain of the NEPSY-II in the Spanish edition (Korkman et al., 2014) assesses figurative language, imitation skills, and the capacity to comprehend the thoughts, ideas, and beliefs of others and it also evaluates a person's capacity to comprehend how emotions relate to the social context.

  3. Social cognition - Theory of mind - Happé's Strange Stories [3 months after the intervention]

    The Happé's Strange Stories Test is a well-known test of ToM (Happé, 1994; Spanish version: Pousa, 2002). In this study, we used the White et al. (2009) version that has eight story-types. This test evaluates participants capacity to comprehend nonliteral meanings through the reading of brief vignettes.

  4. Social cognition - Theory of mind - RMETC [3 months after the intervention]

    The Reading the Mind in the Eyes test Child version (RMETC) (Baron-Cohen et al., 2001; Spanish version: Rueda et al., 2013), is a TOM test that features 28 photos of individuals. The participant's task is to match the picture with one of the four adjectives that best describes the feelings and thoughts of the person in the picture.

Secondary Outcome Measures

  1. Health-related quality of life [3 months after the intervention]

    How an individual's health status impacts their overall well-being and ability to lead a satisfying life The perception of HRQoL is assessed in both healthy and chronically ill children using the Spanish version of the Pediatric Quality of Life Inventory (PedsQLTM 4.0) (Varni et al., 2001). We used the self-report questionnaire in this study for three age ranges: 5-7, 8-12, and 13-18. Physical functioning, emotional functioning, social functioning, and academic functioning are the four dimensions covered by the 23-item assessment. The PedsQL 4.0 provides a physical and a psychosocial summary score in addition to a total score. It is answered through a likert scale with 5 response options that are then converted into quantitative scores ranging from 0-100 points, with a higher score being a better HRQoL.

  2. Psychopathology [3 months after the intervention]

    Behavioral and emotional symptoms The Child Behavior Checklist for Ages 6-18 (CBCL/6-18) (Achenbach & Rescorla, 2001) is a multiaxial assessment tool for identifying behavioral and emotional issues in children and adolescents that is aligned with the ASEBA (Achenbach System of Empirically Based Assessment). It has 113 items total, broken down into eight scales for the following syndromes: anxious/depressed, withdrawn/depressed, somatic complaints, social problems, thinking problems, attention problems, rule-breaking behavior and aggressive behavior. Scores for internalizing, externalizing, and overall difficulties are also provided by the items.

  3. Coping strategies - EAN [3 months after the intervention]

    Different styles to deal with stressful situations Coping Scale for Children (EAN) (Morales-Rodríguez et al., 2012) is a self-report scale assesses coping strategies and is intended for children aged nine to 12 years. In the instrument, four problems related to the family context, health, schoolwork and social relationships are posed. The nine coping strategies assessed are distinguished between problem-focused coping and unproductive coping.

  4. Coping strategies - ACS [3 months after the intervention]

    Different styles to deal with stressful situations Adolescent Coping Scales (ACS) (3rd edition) (Frydenberg and Lewis, 2000): assesses different coping strategies in adolescents aged 12-18 years to cope with their problems. The inventory assesses 18 different coping strategies and consists of 80 items, 79 closed-ended and one open-ended. Furthermore, the 18 strategies are classified into three basic coping styles: problem-directed coping, coping in relation to others, and unproductive coping.

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • To be diagnosed with a neuromuscular disease by a specialist

  • Being between 7 and 16 years old

  • Having signed an informed consent form through their legal guardians prior to participation in the study

  • Having Spanish as one of their main languages

  • Having access to a computer (with a camera, microphone and speakers integrated) and Internet connection to take part in the videoconferences

Exclusion Criteria:
  • Presence of any other diagnosis or sensory deficit that would prevent the application of the tests or hinder the correct performance of the intervention´s activities

  • Being illiterate

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Deusto Bilbao Bizkaia Spain 48007

Sponsors and Collaborators

  • University of Deusto

Investigators

  • Principal Investigator: Oscar Martínez, PhD, University of Deusto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Deusto
ClinicalTrials.gov Identifier:
NCT06031701
Other Study ID Numbers:
  • Neuro-e-Motion NMD
First Posted:
Sep 11, 2023
Last Update Posted:
Sep 11, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 11, 2023