RR with prompting results in a higher rate of self-initiated toileting and a decrease in urinary/faecal accidents. For children who do not attain continence with RR and prompting alone, an add-on restoring procedure will result in a higher rate of…
ID
Bron
Verkorte titel
Aandoening
Day-time urinary incontinence (DUI) and non-retentive faecal incontinence (NFI)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
self-initiated toileting and urinary/faecal accidents during treatment/post-intervention
Achtergrond van het onderzoek
Children and adolescents with neurodevelopmental disabilities seldom attain continence for urine and faeces through maturation. One-to-one training is often needed to establish continence. There is international consensus about the use of least-to-most intrusive treatment procedures for children with Elimination Disorders (ED) with Standard Urotherapy (SU) being considered a first-line treatment. However, specific guidelines pertaining to additional low intrusive procedures, while still producing the desired effect of attaining continence, are lacking in the literature. Furthermore, few studies describe the content of SU interventions and the effectiveness of SU specifically pertaining to children and adolescents with neurodevelopmental disabilities (ND). This PhD study focusses on adhering to the least-to-most intrusive guidelines for treatment and determining the effectiveness of standard urotherapy, behavioural training procedures based on response restriction and a restoring procedure.
Research question
What is the effectiveness of RR training with prompting on DUI/NFI in children and adolescents with ND? What is the effectiveness of an add-on training consisting of a restoring procedure, for children who do not attain self-initiated toileting with RR training plus prompting alone?
Participant characteristics and setting
Twelve participants (5-18 y) will participate in this study. The intervention and add-on sessions will be conducted in a therapy room, 3 x 3m, at SeysCentra. Adjacent to the therapy room is a toilet room, 1,5 x 1,5m. In the therapy room is a table, two chairs, and a cupboard.
Study design
A non-concurrent multiple probe design across participants (Kazdin, 2011) will be used to investigate the effectiveness of RR with prompting and the add-on training consisting of a restoring procedure on DUI and/or NFI in participants.
Procedures
For informed consent, see study 1. Parents will measure urinary/faecal accidents, self-initiated toileting habits at home during at least five probe sessions (baseline). After the home baseline measurement, the participant visits the training centre for 3 additional probe sessions measured by a therapist.
Informed consent of parents and child (>12 y) for this study will be obtained. Participants will visit the training centre for ten workdays (no weekends) from 9:00 AM to 3:00 PM for RR training with prompting during five sessions (phase B). Protocolized RR will be using prompting and ABA procedures. Participants who do not attain a predetermined criterion after five training sessions, will receive an add-on training consisting of a restoring procedure and positive practice for an additional five sessions (phase C). Participants will continue with the treatment procedure without the addition of the restoring procedure, when RR with prompting is effective based on reaching criteria after training session five. Participants who do reach criterion after five sessions in phase C, will continue treatment as outlined in phase C for the remaining training sessions at SeysCentra. After week 2 of training, post-intervention will start. During post-intervention, parents will foster generalization in the natural environment (e.g., at home) of the participant. Parents will receive protocolled feedback and instruction. The post-intervention will end after a pre-set criterion will be reached or after 10 weeks. Eight weeks following post-intervention maintenance will be measured in the follow-up phase for three days. Parents will not receive any feedback or instructions.
Measures and materials
Parents will be asked to measure urinary/faecal accidents, self-initiated toileting habits at home for at least five probes during the baselines, post-intervention, and follow-up. Event recording during a morning session (9:00 AM-12:00PM) and afternoon session (12:00 PM – 3:00 PM) of urinary/faecal accidents and self-initiated toileting habits (rate per 3 hours) will be conducted. Data on procedural fidelity will be collected by an independent observer (i.e., research assistant) in 30% of all sessions across participants during the treatment phase. Interobserver agreement will be calculated using mean count per three hours. Procedural fidelity of VM and RR will be calculated per session based on the ratio of executed components versus planned components.
Doel van het onderzoek
RR with prompting results in a higher rate of self-initiated toileting and a decrease in urinary/faecal accidents. For children who do not attain continence with RR and prompting alone, an add-on restoring procedure will result in a higher rate of self-initiated toileting and a decrease in urinary/faecal accidents.
Onderzoeksopzet
Rate of self-initiated toileting and urinary/faecal accidents at the end of:
- Baseline 1
- SU
- Baseline 2
- Intervention
- Post-intervention
- Follow-up
Onderzoeksproduct en/of interventie
Restoring procedure
Response Restriction (RR) with prompting
Standard Urotherapy (SU)
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
All participants meet the following inclusionary criteria: They (a) have DUI, assessment and diagnosis using ICCS criteria (von Gontard, 2013b; Austin et al., 2016), and/or (b) have NFI, assessment and diagnosis using Rome IV criteria (von Gontard, 2013a; Hyams et al., 2016), (c) underwent a paediatric examination (d) have an IQ ≥35, (e) have ability to stand and walk, (f) have no visual impairment, and (g) SU training at SeysCentra has already been conducted, and did not result in continence.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Participants will be excluded from this research study based on the following exclusion criteria: They (a) have an IQ ≤ 34, (b) are unable to stand or walk, (c) have a visual impairment, (d) do not have NFI or DUI, (e) received a completed SU training according to the ICCS criteria (von Gontard, 2013b) at a different facility, or (f) completed a SU training which was effective in attaining continence.
Opzet
Deelname
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