TreatPaCS = Treatment for Preschool Age Children Who Stutter

Sponsor
Thomas More University of Applied Sciences (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05185726
Collaborator
Universiteit Antwerpen (Other), University of Liege (Other), Artevelde University of Applied Sciences (Other)
249
1
3
43
5.8

Study Details

Study Description

Brief Summary

Treatment for preschool age children who stutter: a randomised, multicentre, non-inferiority parallel group pragmatic trial with Mini-KIDS, the social cognitive behaviour therapy and the Lidcombe Program with 249 children

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Lidcombe Program
  • Behavioral: Mini-KIDS
  • Behavioral: Social Cognitive Behavioural Therapy
N/A

Detailed Description

Three treatment approaches for preschool age children who stutter are delivered and %Syllables Stuttered at 18 months post-randomisation of the three arms are compared .

Mini-KIDS is a direct treatment based on principles of stuttering modification, with pseudo-stuttering, that is, deliberate stuttering, as one of the main components. The program for 4-6-year old children consists of four stages: Stage 1 = desensitization, Stage 2 = modification, Stage 3 = identification and Stage 4 = generalization. The program for 2-4-year old children does not include stage 3. Speech therapist and parent(s) are the speech model for the child. They add normal dysfluencies to their speech. Later on in treatment and if necessary, children learn to recognise and alter their stuttering moments.

The social cognitive behaviour therapy contains 5 treatment phases: (1) conditioning speaking activities, (2) cognitive training focused on emotions, (3) cognitive training focused on cognitions, (4) emotional training and (5) skill training (Boey, 2010). This treatment is not directed at the speech of the children, but rather at the cognitive and emotional aspects that surround the stuttering.

The Lidcombe Program (LP) is an operant program that directly provides verbal feedback to the child's stutter-free speech (mainly) and the child's stuttering (occasionally). The program comprises two stages: Stage 1 in which (near) zero levels of stuttering are achieved and Stage 2 in which the achieved (near) zero levels of stuttering are maintained for a long period of time. The LP usually takes between 11 to 23 (60-minute) treatment sessions to achieve the goals of Stage 1, i. e. (near) zero levels of stuttering.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
249 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A three arm 1:1:1 randomised, multicentre, open-label non-inferiority parallel group pragmatic trialA three arm 1:1:1 randomised, multicentre, open-label non-inferiority parallel group pragmatic trial
Masking:
Single (Outcomes Assessor)
Masking Description:
Videos of speech will be scores for %SS by assessors who are blinded for the treatment arm in which the child belongs.
Primary Purpose:
Treatment
Official Title:
Treatment for Preschool Age Children Who Stutter: A Randomised, Multicentre, Non-inferiority Parallel Group Pragmatic Trial With Mini-KIDS, the Social Cognitive Behaviour Therapy and the Lidcombe Program With 249 Children
Anticipated Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Nov 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mini-KIDS

Mini-KIDS is a direct treatment based on principles of stuttering modification, with pseudo-stuttering, that is, deliberate stuttering, as one of the main components. The program for 4-6-year old children consists of four stages: Stage 1 = desensitization, Stage 2 = modification, Stage 3 = identification and Stage 4 = generalization. The program for 2-4-year old children does not include stage 3. Speech therapist and parent(s) are the speech model for the child. They add normal dysfluencies to their speech. Later on in treatment and if necessary, children learn to recognise and alter their stuttering moments.

Behavioral: Mini-KIDS
Mini-KIDS for 4-6-year old PCWS consists of four stages: Stage 1 = desensitization, Stage 2 = identification, Stage 3 = modification and Stage 4 = generalization. The program for 2-4-year old child does not include stage 2. SLT and parent(s) are the speech model for the child. They add normal disfluencies and pseudo-stuttering to their speech at first to make sure the child dares to stutter and the child as well as the parent(s) are desensitized for it. Later on in treatment and if necessary, child learn to recognise and alter their stuttering moments. The maintenance phase starts when the child and parent(s) achieved the goals of Stage 4. Usually the stuttering is reduced to (near) zero stuttering. Treatment sessions to monitor if achieved goals are maintained are scheduled with an interval of 2, 2, 4, 4, 8, 8 and 16 weeks.

Experimental: Social-Cognitive Behaviour Treatment

The social cognitive behaviour therapy contains 5 treatment phases: (1) conditioning speaking activities, (2) cognitive training focused on emotions, (3) cognitive training focused on cognitions, (4) emotional training and (5) skill training (Boey, 2010). This treatment is not directed at the speech of the children, but rather at the cognitive and emotional aspects that surround the stuttering.

Behavioral: Social Cognitive Behavioural Therapy
A parent training is organised for parents with children who stutters who receive SCBT. The parent training exists of 10 one-hour group evening sessions for parents to discuss and offer education topics about what stuttering is, how stuttering looks like, ... The program is delivered in 5 phases and each phase takes as long as is necessary for the PCWS (variable): (1) conditioning speaking activities, (2) cognitive training focused on emotions, (3) cognitive training focused on cognitions, (4) emotional training and (5) skill training. The maintenance phase starts when the child and parent(s) achieved the goals of the 5 phases. During the maintenance sessions, the SLT asks the parent(s) to report about the child and observes the speech of the child.
Other Names:
  • SCBT
  • Active Comparator: Lidcombe Program

    The Lidcombe Program (LP) is an operant program that directly provides verbal feedback to the child's stutter-free speech (mainly) and the child's stuttering (occasionally). The program comprises two stages: Stage 1 in which (near) zero levels of stuttering are achieved and Stage 2 in which the achieved (near) zero levels of stuttering are maintained for a long period of time. The LP usually takes between 11 to 23 (60-minute) treatment sessions to achieve the goals of Stage 1, i. e. (near) zero levels of stuttering.

    Behavioral: Lidcombe Program
    The LP consists of Stage 1 and Stage 2. Stage 1 aims at reducing the stuttering of the PCWS to (near) zero levels of stuttering. During stage 1, parents learn to provide verbal contingencies during daily, 10-minute practice sessions with their PCWS. During Stage 1, treatment sessions are scheduled weekly. When the child has typical scores of 0 and 1 on the SR-scale with more 0s than 1s per week for three consecutive weeks, and the stuttering is rated as 0 or 1 during the treatment session, the child can proceed to stage 2. The maintenance phase starts when the stuttering is reduced to (near) zero stuttering and parents are able to implement the practice sessions when it is necessary (when stuttering relapses). Treatment sessions to monitor if achieved goals are maintained are scheduled with an interval of 2, 2, 4, 4, 8, 8 and 16 weeks.
    Other Names:
  • LP
  • Outcome Measures

    Primary Outcome Measures

    1. % of Syllables Stuttered (%SS) [18 months post-randomisation]

      The %SS at 18 months post-randomisation will be determined in two video samples (at home and in the treatment session) and the average will be used. They will be conpared between the 3 programs.

    Secondary Outcome Measures

    1. Severity rating of the stuttering [3-, 6-, 9-, 12-, 18-months and 2- and 5-year post-randomisation]

      The severity rating of the stuttering will be averaged over home and treatment session and will be compared between the 3 programs

    2. Speech attitude (Kiddy CAT) scores [18-months post-randomisation]

      Score on the KiddyCAT will be compared between the 3 programs

    3. Score on Quality of life questionnaire [at 18-months, 2- and 5-years post-randomisation]

      Score on the EQ-5D-Y-proxy 2 will be compared between the 3 programs

    4. Score on Impact of Stuttering on Parents and Preschooler (ISPP) questionnaire [at 18-months post-randomisation]

      Score on the ISPP will be compared between the 3 programs

    5. % of Syllables Stuttered (%SS) [3-, 6-, 9-, 12-months and 2- and 5-year post-randomisation]

      The %SS will be determined in two video samples (at home and in the treatment session) and the average will be used. They will be conpared between the 3 programs.

    6. Treatment duration (number of hours) [Through study completion, on average 9 months]

      Treatment duration will be calculated in number of hours

    7. Treatment duration (number of weeks) [Through study completion, on average 9 months]

      Treatment duration will be calculated in number of weeks

    8. Treatment duration (number of sessions) [Through study completion, on average 9 months]

      Treatment duration will be calculated in number of weeks

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    24 Months to 78 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    Preschool age children must

    • stutter (identified by the Speech-Language Therapist)

    • be aged between 2 - 6.5 years

    • have normal hearing reported by the parent(s)

    • have, if bilingual, a parent who speaks a language that the SLT understands and speaks to allow clear communication

    • have at least one parent agreeing to be intensively involved in treatment and knowing that s/he will implement treatment at home

    • have at least one parent who is willing and able to videorecord his/her child regularly

    Exclusion Criteria:
    • have a syndrome such as Down Syndrome.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sabine Van Eerdenbrugh Antwerpen Belgie Belgium 2000

    Sponsors and Collaborators

    • Thomas More University of Applied Sciences
    • Universiteit Antwerpen
    • University of Liege
    • Artevelde University of Applied Sciences

    Investigators

    • Principal Investigator: Sabine Van Eerdenbrugh, Dr, Thomas More

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Thomas More University of Applied Sciences
    ClinicalTrials.gov Identifier:
    NCT05185726
    Other Study ID Numbers:
    • M-OHC-210048
    First Posted:
    Jan 11, 2022
    Last Update Posted:
    Jan 11, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    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 Jan 11, 2022