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DEVELOPMENT OF TRAINING PROTOCOL AND APPLICATION FOR SPEECH LANGUAGE PATHOLOGISTS ON TELETHERAPY: A CONTEMPORARY APPROACH TO SPEECH LANGUAGE THERAPY

9 settembre 2026 aggiornato da: University of Lahore

The goal of this mixed-methods study is to develop and evaluate a teletherapy training protocol and a dedicated teletherapy application for Speech-Language Pathologists (SLPs) in Pakistan. It will also assess the effectiveness, usability, and acceptability of these tools among SLPs and patients receiving speech-language therapy services. The main questions it aims to answer are:

Can a standardized teletherapy training protocol be developed and validated for Speech-Language Pathologists? Can a teletherapy application improve the delivery and effectiveness of speech-language therapy services? What are the perceptions, experiences, and satisfaction levels of SLPs and patients regarding teletherapy? Does the use of the developed protocol and application improve the quality and accessibility of speech-language therapy services?

Researchers will assess the effectiveness of the developed protocol and application by comparing outcomes before and after implementation among Speech-Language Pathologists and patients receiving teletherapy services.

Participants will:

Complete questionnaires regarding teletherapy practices, satisfaction, effectiveness, and challenges.

Participate in structured interviews to share experiences and perceptions of teletherapy.

Contribute to the development and validation of a teletherapy training protocol through expert consultation.

Use the developed teletherapy application for speech and language intervention. Participate in evaluations to assess the effectiveness, usability, and acceptability of the protocol and application.

The expected outcome of the study is the development of a validated teletherapy protocol and a comprehensive teletherapy application that can standardize telepractice and improve the accessibility and quality of speech-language pathology services in Pakistan.

Panoramica dello studio

Descrizione dettagliata

Teletherapy has emerged as an important mode of service delivery in speech-language pathology, particularly following the COVID-19 pandemic. Although teletherapy has been increasingly adopted worldwide, many Speech-Language Pathologists (SLPs) continue to face challenges related to the absence of standardized training, limited technological resources, and inconsistent clinical practices. In Pakistan, teletherapy services are being utilized by practitioners; however, there is currently no validated training protocol or comprehensive teletherapy application specifically designed to support speech-language pathology services.

This study aims to develop a standardized teletherapy training protocol and a dedicated teletherapy application for Speech-Language Pathologists. The study will employ a mixed-methods approach involving quantitative surveys and qualitative interviews with practicing SLPs to identify current teletherapy practices, challenges, training needs, and recommendations. Findings from these phases will be used to develop a protocol through expert consensus using the Delphi technique.

The proposed protocol will address essential operational and ethical aspects of teletherapy, including clinician competencies, client eligibility, technology requirements, service delivery procedures, documentation practices, privacy and confidentiality, informed consent, and quality assurance measures. Following protocol development, a teletherapy application will be designed to facilitate the delivery of speech and language intervention services for a range of communication disorders.

The psychometric properties of the developed protocol, including validity and reliability, will be evaluated. Subsequently, the protocol and application will be implemented in clinical practice to assess their effectiveness, usability, and acceptability among both clinicians and service recipients. Outcome measures will focus on user satisfaction, perceived effectiveness, feasibility, and the overall quality of teletherapy service delivery.

The anticipated outcome of this research is the establishment of an evidence-based framework for teletherapy in speech-language pathology, supported by a practical digital application. The findings are expected to contribute to the standardization of teletherapy practices, enhance access to speech-language services, and support the integration of telepractice into routine clinical care in Pakistan and similar healthcare settings.

Tipo di studio

Interventistico

Iscrizione (Stimato)

10

Fase

  • Non applicabile

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

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  • • The inclusion criteria will include Speech Language Pathologists from Pakistan that are actively involved in the profession.

    • Speech language pathologists with minimum qualification of undergraduate degree in Speech language pathology and licensed SLP's working with patients through teletherapy mode will be included in the study.
    • SLP's dealing with speech, language and communication problems will be included in the study.
    • The patients or their guardians currently receiving speech language pathology services.
    • Any age range of patients or guardians will be included in the study.

Exclusion Criteria:

  • • The exclusion criteria will not involve seminars or academic activities; it will not consider the therapeutic interventions used by other counselling or session-based therapists i.e., psychologists.

    • Patients with psychological, visual impairment, physical limitations, and medical conditions such as cancer and other long-term diseases will be excluded from the study.
    • The patients with swallowing disorder are excluded in the study.

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: App-supported teletherapy
Speech and language therapy delivered through weekly live video sessions with a speech-language pathologist trained in the study teletherapy protocol, supported by the TeleSpeech application for home practice. One 30-45 minute session per week for 12 weeks plus a home programme assigned in the application and practised on five days per week. Delivered in the participant's home or a quiet room at the site.
Speech and language therapy delivered by a speech-language pathologist through scheduled live video sessions, supported by the TeleSpeech progressive web application for home practice. One 30 to 45 minute individual session per week for 12 weeks, delivered in the participant's home or in a quiet room at the site where the family prefers that. Between sessions, a home programme is assigned in the application by the treating therapist and practised on five days per week. Therapy content and targets are individualised. The treating therapist has completed the study teletherapy training protocol. Adherence is captured automatically by the application, which timestamps each login, activity and completion, and session attendance is logged.
Comparatore attivo: Usual in-person therapy
Standard face-to-face speech and language therapy as currently delivered at the site by a speech-language pathologist in usual practice. One 30-45 minute session per week for 12 weeks plus a paper home programme practised on five days per week. Delivered in the clinic.
Standard face-to-face speech and language therapy as currently delivered at the participating site by a speech-language pathologist in usual practice. One 30 to 45 minute individual session per week for 12 weeks, delivered in the clinic. Between sessions, a home programme is given to the family on paper and practised on five days per week. Therapy content and targets are individualised as in usual practice. Adherence is recorded in a paper diary returned at each session, and attendance is logged from site records.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Goal Attainment Scaling (GAS) T-score
Lasso di tempo: Baseline and 12 weeks after randomisation (change from baseline to 12 weeks)
Goal Attainment Scaling is a criterion-referenced method in which three to five individually agreed therapy goals are set with the participant and family before randomisation and scaled from -2 (much less than expected) to +2 (much more than expected), with 0 as the expected level of attainment. Goals are not revised after randomisation. Attainment is rated at 12 weeks by an outcome assessor masked to allocation and converted to a standardised T-score. Higher scores indicate greater attainment of individually agreed communication goals. The outcome reported is the change in T-score from baseline to 12 weeks, analysed by analysis of covariance with the baseline value, site and diagnostic group as covariates. Non-inferiority of app-supported teletherapy will be concluded if the lower bound of the two-sided 95% confidence interval for the between-arm difference lies above the pre-specified margin..
Baseline and 12 weeks after randomisation (change from baseline to 12 weeks)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Adherence to the prescribed home practice programme
Lasso di tempo: Weekly over the 12-week intervention period
The proportion of prescribed home-practice days on which practice was completed, over the 12-week intervention period, expressed as a percentage. In the app-supported teletherapy arm this is derived from timestamps recorded automatically by the application. In the usual in-person therapy arm it is derived from a paper practice diary returned at each session. The difference in measurement method between arms is recognised and is reported as a limitation
Weekly over the 12-week intervention period
Proportion of scheduled therapy sessions attended
Lasso di tempo: Over the 12-week intervention period
The number of therapy sessions attended as a proportion of the number scheduled over the 12-week intervention period, expressed as a percentage, taken from site attendance records in both arms. A session is counted as attended if it began, whatever its duration.
Over the 12-week intervention period
Client Satisfaction Questionnaire (CSQ-8) score
Lasso di tempo: 12 weeks after randomisation
Participant or caregiver satisfaction with the therapy received, measured on the eight-item Client Satisfaction Questionnaire. Total scores range from 8 to 32, with higher scores indicating greater satisfaction. Self-reported, or reported by the caregiver where the participant is a child or is unable to self-report.
12 weeks after randomisation
System Usability Scale (SUS) score
Lasso di tempo: 12 weeks after randomisation
Usability of the TeleSpeech application, measured on the ten-item System Usability Scale. Scores range from 0 to 100, with higher scores indicating better perceived usability. Collected from participants or caregivers in the app-supported teletherapy arm only, as participants in the usual in-person therapy arm do not use the application.
12 weeks after randomisation

Collaboratori e investigatori

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

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)

20 settembre 2026

Completamento primario (Stimato)

20 marzo 2027

Completamento dello studio (Stimato)

20 aprile 2027

Date di iscrizione allo studio

Primo inviato

9 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

9 settembre 2026

Primo Inserito (Effettivo)

15 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

9 settembre 2026

Ultimo verificato

1 gennaio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • REC-UOL-/574/08/24
  • University of Cyberjaya (Identificatore di registro: University of Cyberjaya)

Piano per i dati dei singoli partecipanti (IPD)

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

INDECISO

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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