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Acceptability of FitSkills in the Irish Context for Young People With Childhood-onset Physical Disability

10 luglio 2026 aggiornato da: Royal College of Surgeons, Ireland

The Feasibility and Acceptability of Translating FitSkills to the Irish Context to Facilitate Physical Activity Participation for Young People With Childhood-onset Physical Disability

FitSkills is an evidence based community based gym programme developed in Australia. It was developed in response to the barriers people with disability experience to accessing community-based physical activity. Within FitSkills, people with disability are paired with university students who act as a peer mentor. Pairs exercise together at a community gym location twice a week for 12 weeks. FitSkills has been shown to improve physical and social health among people with disabilities.

FitSkills has not been delivered outside of Australia. The investigators are assessing how practical it is to deliver FitSkills in Ireland with the support of healthcare and physical activity professionals. The investigators want to understand the demand for this programme among young people with childhood-onset physical disability aged 13-24 years. In addition, the investigators want to learn if taking part in FitSkills influences exercise confidence and mental health and well-being among young people with childhood-onset physical disability.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

25

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

Backup dei contatti dello studio

  • Nome: Ailish Malone, PhD

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

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Have a primary physical disability diagnosis, either congenital or acquired by age 15
  • Are aged between 13-24 years
  • Have not taken part in a regular gym programme in the previous 3 months (i.e. at least once a week for 3 months)
  • Can follow instructions in English
  • Are fit and well enough to participate in exercise

Exclusion Criteria:

  • Have an acute or concurrent medical condition rendering them unfit to participate in moderate-level physical activity
  • If they had an impaired ability to take part safely in a gym environment due to significant behavioural challenges.

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: Ricerca sui servizi sanitari
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Altro: FitSkills
FitSkills- Community-based physical activity programme
12 week community gym exercise programme. Twice weekly gym sessions for 60 minutes. Peer support provided by a third level healthcare student from host university. Standardised exercise programme developed by gym staff with support from the investigators. Goals and preferences of participants considered in programme development. This is the only intervention and there is no additional intervention provided

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Participant recruitment (Reach)
Lasso di tempo: Up to 6 months from study opening for recruitment

Participant recruitment (reach) will be assessed by the number of individuals who express interest in the study and the proportion who are eligible and enrolled.

Additional descriptive data will be collected on recruitment, including the number of enquiries and completed expressions of interest, how participants heard about the study (e.g., healthcare professional referral, flyer, or other sources), eligibility outcomes (number eligible, number excluded, and reasons for exclusion), and basic demographic characteristics (age, gender, disability type, and location) of individuals expressing interest.

Up to 6 months from study opening for recruitment
Adoption by healthcare and physical activity professionals
Lasso di tempo: Up to 7 months from first participant initiation of the intervention

Adoption will be assessed by the number and proportion of healthcare and physical activity professionals who are invited and agree to support implementation of the intervention.

Additional descriptive data will be collected on professional characteristics (e.g., profession, service type, public or private service, and service location) and reasons for non-participation (e.g., work capacity constraints or lack of interest).

Up to 7 months from first participant initiation of the intervention
Intervention Feasibility
Lasso di tempo: Up to 7 months from first participant initiation of the intervention

Intervention feasibility will be assessed by the proportion of participant pairs who complete the programme at 12 weeks.

Additional descriptive data will be collected, including the number of pairs successfully matched (young people and student mentors), the number attending the group orientation session, and participant engagement (e.g., use of the challenge board).

Fidelity to programme content and adverse events will be monitored and recorded using exercise log-books.

Up to 7 months from first participant initiation of the intervention
Feasibility of the Intervention (Feasibility Intervention Measure)
Lasso di tempo: At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)

Feasibility will be assessed using the Feasibility of Intervention Measure (FIM), completed by healthcare and physical activity professionals following completion of their involvement in implementation.

The FIM is a 4-item scale assessing perceived feasibility (e.g., whether the programme is possible, practical, and easy to implement), with responses rated on a 5-point Likert scale ranging from completely disagree to completely agree.

At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)
Feasibility of collaboration between professionals
Lasso di tempo: Up to 7 months from first participant initiation of the intervention

Feasibility of collaboration between healthcare and physical activity professionals will be assessed using a communication logbook completed by professionals involved in implementation.

The logbook will capture the number of contacts between professionals and characteristics of communication, including reason for contact, type of communication, and outcome of communication.

Up to 7 months from first participant initiation of the intervention
Acceptability of the intervention among professionals
Lasso di tempo: At completion of the intervention (up to 7 months from first participant initiation)

Acceptability of the intervention will be assessed through online focus groups conducted with healthcare and physical activity professionals following implementation.

Focus groups will explore participants' perceptions of the acceptability of the programme, including its perceived appropriateness, burden, and satisfaction with implementation.

At completion of the intervention (up to 7 months from first participant initiation)
Acceptability of the intervention ( Acceptability of Intervention Measure)
Lasso di tempo: At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)

Acceptability will be assessed using the Acceptability of Intervention Measure (AIM), completed by healthcare and physical activity professionals.

The AIM is a 4-item scale assessing perceived acceptability (e.g., whether the programme is appealing, meets approval, and is welcomed), with responses rated on a 5-point Likert scale ranging from completely disagree to completely agree.

At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)
Appropriateness of the intervention ( Intervention Appropriateness Measure)
Lasso di tempo: At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)

Appropriateness will be assessed using the Intervention Appropriateness Measure (IAM), completed by healthcare and physical activity professionals.

The IAM is a scale assessing perceived appropriateness (i.e., the extent to which the programme is suitable and relevant), with responses rated on a 5-point Likert scale ranging from completely disagree to completely agree.

At completion of professional involvement in intervention implementation (up to 7 months from first participant initiation)
Acceptability of the intervention among young people
Lasso di tempo: At completion of the intervention (up to 7 months from first participant initiation)

Acceptability of the intervention will be assessed through online semi-structured interviews conducted with young people with disability who participated in the programme.

Interviews will explore participants' perceptions of acceptability, including satisfaction with the programme, perceived benefits, and burden of participation.

At completion of the intervention (up to 7 months from first participant initiation)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Exercise self efficacy ( Exercise Self Efficacy Scale)
Lasso di tempo: Baseline (prior to intervention initiation) and at 12 weeks (end of intervention)

Exercise self-efficacy will be assessed using the Exercise Self-Efficacy Scale, completed by young people with childhood-onset physical disability.

The scale consists of 10 items assessing confidence in engaging in physical activity, with responses rated on a 4-point Likert scale (not at all true, rarely true, sometimes true, always true). Total scores range from 10 to 40, with higher scores indicating greater exercise self-efficacy.

Baseline (prior to intervention initiation) and at 12 weeks (end of intervention)
Mental health and well-being (Mental Health Continuum-Short Form)
Lasso di tempo: Baseline (prior to intervention initiation) and at 12 weeks (end of intervention)

Mental health and well-being will be assessed using the Mental Health Continuum-Short Form (MHC-SF), completed by young people with childhood-onset physical disability.

The MHC-SF assesses emotional, social, and psychological well-being using a 6-point Likert scale (1 = everyday to 6 = never). Scores can be interpreted using continuous total and domain scores, with higher scores indicating greater well-being. Participants may also be classified as flourishing, moderately mentally healthy, or languishing based on established scoring criteria.

Baseline (prior to intervention initiation) and at 12 weeks (end of intervention)

Collaboratori e investigatori

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

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

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)

1 luglio 2026

Completamento primario (Stimato)

1 gennaio 2027

Completamento dello studio (Stimato)

1 gennaio 2027

Date di iscrizione allo studio

Primo inviato

27 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 luglio 2026

Primo Inserito (Effettivo)

14 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

14 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 luglio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 202510045

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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