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

2026년 7월 10일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

25

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

  • 이름: Ailish Malone, PhD

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 건강 서비스 연구
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
다른: 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

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Participant recruitment (Reach)
기간: 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
기간: 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
기간: 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)
기간: 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
기간: 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
기간: 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)
기간: 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)
기간: 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
기간: 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)

2차 결과 측정

결과 측정
측정값 설명
기간
Exercise self efficacy ( Exercise Self Efficacy Scale)
기간: 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)
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 7월 1일

기본 완료 (추정된)

2027년 1월 1일

연구 완료 (추정된)

2027년 1월 1일

연구 등록 날짜

최초 제출

2026년 5월 27일

QC 기준을 충족하는 최초 제출

2026년 7월 10일

처음 게시됨 (실제)

2026년 7월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 10일

마지막으로 확인됨

2026년 5월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • 202510045

약물 및 장치 정보, 연구 문서

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미국 FDA 규제 기기 제품 연구

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이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .