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Evaluating ICF-Based Case Management in Adults With Intellectual Disabilities

5 novembre 2026 aggiornato da: Po Leung Kuk

Effectiveness of ICF-based Case Management in Promoting Independence and Vocational Participation Among Adults With Intellectual Disabilities: A Randomized Controlled Trial

The goal of this clinical trial is to evaluate whether an ICF-based interdisciplinary case management model can improve adaptive functioning, functioning and participation, and vocational functioning among adults aged 18 to 60 years with mild to moderate intellectual disabilities receiving residential care or vocational rehabilitation services in Hong Kong. The main questions it aims to answer are:

  • Does ICF-based interdisciplinary case management lead to greater improvements in adaptive functioning, as measured by the Vineland Adaptive Behavior Scales, Third Edition (Vineland-3), compared with conventional multidisciplinary rehabilitation care?
  • Does ICF-based interdisciplinary case management improve functioning and participation outcomes across relevant ICF domains compared with conventional multidisciplinary rehabilitation care?
  • Among participants receiving vocational rehabilitation services, does the intervention improve vocational functioning and work-related behaviours compared with conventional multidisciplinary rehabilitation care?

Researchers will compare participants receiving ICF-based interdisciplinary case management with those receiving conventional multidisciplinary rehabilitation care to determine whether the ICF-based approach produces better outcomes in adaptive functioning, functioning and participation, and vocational functioning.

Participants will:

  • Complete baseline and post-intervention assessments over a 6-month study period.
  • Be randomly assigned to either the ICF-based case management group or the conventional care group.
  • Receive rehabilitation services from multidisciplinary professionals.
  • If assigned to the intervention group, undergo ICF-based assessment, interdisciplinary goal setting, case conferences, and coordinated rehabilitation planning guided by the ICF Rehab-Cycle®.
  • Complete outcome evaluations using the Vineland-3, WHO ICF Checklist v2.1a, and, where applicable, the Chinese Work Personality Profile (CWPP).

Panoramica dello studio

Descrizione dettagliata

Adults with intellectual disabilities often experience complex and interrelated challenges in adaptive functioning, participation, and community integration that require coordinated interdisciplinary rehabilitation. The World Health Organization's International Classification of Functioning, Disability and Health (ICF) provides a biopsychosocial framework for understanding functioning and disability and facilitates communication, goal setting, and collaborative care planning among rehabilitation professionals.

This randomized controlled trial aims to evaluate the effectiveness of an ICF-based interdisciplinary case management model for adults with intellectual disabilities receiving residential care or vocational rehabilitation services. Participants will be randomly allocated to either an ICF-based interdisciplinary case management group or a conventional multidisciplinary rehabilitation care group and followed for six months.

The intervention is guided by the ICF Rehab-Cycle®, which comprises four key processes: assessment, assignment, intervention, and evaluation. Using the ICF framework, interdisciplinary team members will conduct a comprehensive assessment of participants' body functions, activities, participation, environmental factors, and personal factors. Assessment findings will be used to develop a shared understanding of each participant's functioning profile and to formulate individualized rehabilitation goals through interdisciplinary case conferences. These goals will guide coordinated intervention planning and service delivery. Participants' progress and goal attainment will be reviewed regularly, and intervention strategies will be adjusted according to changes in functioning and participation throughout the rehabilitation process.

Participants in the control group will receive routine multidisciplinary rehabilitation services according to existing service practices without the use of a structured ICF-based case management framework.

The findings will provide evidence regarding the clinical effectiveness and feasibility of implementing an ICF-based interdisciplinary case management approach in intellectual disability rehabilitation services and may inform future service development, interdisciplinary practice, and the application of the ICF framework in rehabilitation settings.

Tipo di studio

Interventistico

Iscrizione (Stimato)

84

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Hong Kong, Hong Kong, 999077
        • Po Leung Kuk Lau Chan Siu Po Integrated Rehabilitation Centre
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 60 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

To be eligible for participation, individuals must:

  1. be aged between 18 and 60 years;
  2. have a formal medical diagnosis of mild or moderate intellectual disability;
  3. be currently receiving residential care or vocational rehabilitation services;
  4. be medically stable and able to participate in routine rehabilitation programmes; and
  5. provide informed consent directly or via a legally authorized representative.

Individuals will be excluded if they:

  1. experience an acute or unstable medical condition requiring intensive treatment;
  2. present with acute psychiatric episodes that may substantially interfere with participation;
  3. are currently participating in ICF-Based Interdisciplinary Case Management Programme; or
  4. lack an available consent pathway through either personal consent or legal representation.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: ICF-Based Interdisciplinary Case Management

Participants will receive rehabilitation services coordinated using the International Classification of Functioning, Disability and Health (ICF) framework. The intervention includes standardized ICF-based assessment, interdisciplinary case conferences, collaborative goal setting, individualized rehabilitation planning, and coordinated intervention delivery by multidisciplinary team members over a 6-month period. Outcomes are monitored and reviewed according to participants' functioning, participation, environmental, and personal factors.

A structured case management model utilizing the ICF framework to guide assessment, goal setting, intervention planning, and interdisciplinary collaboration for adults with intellectual disabilities receiving rehabilitation services.

Comparatore attivo: Conventional Multidisciplinary Rehabilitation Care

Participants will receive usual rehabilitation services provided by multidisciplinary professionals according to existing service practices. Assessment, goal setting, and intervention planning will be conducted in accordance with routine procedures without the use of a structured ICF-based case management framework.

Standard rehabilitation services delivered by multidisciplinary professionals, including discipline-specific assessment, rehabilitation planning, and intervention based on existing service protocols.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Adaptive Functioning
Lasso di tempo: Baseline and 6 months (post-intervention)

Adaptive functioning measured by the Vineland Adaptive Behavior Scales, Third Edition (Vineland-3). The Vineland-3 assesses participants' adaptive behavior across domains including communication, daily living skills, and socialization. Change in scores from baseline to 6 months will be compared between the intervention and control groups.

Baseline and 6 months (post-intervention)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Functioning and Participation
Lasso di tempo: Baseline and 6 months post-intervention.

Functioning and participation measured using the WHO ICF Checklist Version 2.1a. The assessment evaluates functioning across body functions, activities and participation, environmental factors, and personal factors. Changes from baseline to 6 months will be compared between groups.

Baseline and 6 months post-intervention.
Vocational Functioning
Lasso di tempo: Baseline and 6 months post-intervention.

Vocational functioning measured using the Chinese Work Personality Profile (CWPP). The assessment evaluates work-related behaviors and vocational performance among participants receiving vocational rehabilitation services. Changes from baseline to 6 months will be compared between groups.

Baseline and 6 months post-intervention.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

26 novembre 2026

Completamento primario (Stimato)

30 settembre 2027

Completamento dello studio (Stimato)

30 ottobre 2027

Date di iscrizione allo studio

Primo inviato

5 novembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

5 novembre 2026

Primo Inserito (Effettivo)

12 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

5 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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