Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Reablement Intervention for Older Adults in Day Care Centers

23 aprile 2026 aggiornato da: National Taiwan University Hospital

Reablement Intervention for Older Adults With Functional Decline in Day Care Centers: An Exploratory Quasi-Experimental Study Comparing Exercise Intervention

This study explores the effectiveness of reablement interventions for older adults with declining mobility in adult day care centers and compares them with traditional exercise interventions. In recent years, reablement has gained increasing attention. It is a person-centered approach that emphasizes goal-oriented training through activities of daily living, combined with interdisciplinary collaboration, to enhance individuals' self-care abilities and participation in daily life. In contrast, exercise interventions are typically structured programs focusing on improving muscle strength, balance, and endurance. While both approaches aim to enhance physical function, they differ in philosophy, implementation context, and motivational mechanisms. Reablement emphasizes meaningful, individualized, and context-based activities, which may enhance motivation and adherence, whereas exercise interventions are more standardized and efficient but may lack relevance to daily life, potentially affecting long-term engagement.

This study adopts a quasi-experimental design to compare the effects of reablement and exercise interventions on mobility, fear of falling, activities of daily living, and subjective well-being among older adults. It also evaluates the feasibility of implementing reablement in day care centers. Additionally, participants' preferences, attendance, and engagement in different intervention approaches are examined to address the current gap in comparative research.

Overall, the findings suggest that incorporating reablement into day care services-through individualized goal setting and interdisciplinary collaboration-can enhance functional performance, quality of life, and independence among older adults. The results also provide important evidence for future long-term care policy and practice, supporting a shift from a care-oriented model to a function-oriented approach, and ultimately promoting aging in place and independent living.

Panoramica dello studio

Stato

Attivo, non reclutante

Tipo di studio

Interventistico

Iscrizione (Effettivo)

80

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.

Luoghi di studio

      • Taipei, Taiwan
        • National Taiwan University

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

  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Aged 65 years or older and assessed as Long-Term Care (LTC) need level 2 or above.
  • Regularly attending adult day care services at least two days per week, with no anticipated termination of services during the study period (approximately three months).
  • Short Portable Mental Status Questionnaire (SPMSQ) results indicating intact, mild, or moderate cognitive impairment, with the ability to understand simple instructions and participate in activities with assistance.
  • Able to ambulate independently (assistive devices permitted), with a Short Physical Performance Battery (SPPB) score < 9, indicating functional decline and high risk of falls.
  • A score ≥ 9 on the Short Falls Efficacy Scale International (Short FES-I), indicating at least moderate fear of falling.
  • Willing to participate in the study and able to provide written informed consent.

Exclusion Criteria:

  • History of fracture, major fall, or need for acute medical treatment within the past three months, or deemed by a physician to be unsuitable for moderate or higher levels of physical activity.
  • Presence of acute psychiatric symptoms that prevent participation in assessments or study procedures.
  • Severe visual or hearing impairments that interfere with activity participation or assessment.
  • Currently receiving other intensive rehabilitation or participating in another research intervention.
  • Demonstrates a clear lack of willingness to participate in the intervention or is unable to complete the three-month observation period.

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: Non randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Reablement intervention

Based on the principles of reablement care and incorporating the Person-Environment-Occupation (PEO) model, the intervention is designed according to older adults' individual preferences, life experiences, and functional needs. It consists of context-based, function-oriented activities embedded in daily life situations.

The intervention is delivered in small groups (5-10 participants per group), where individualized reablement activities are implemented alongside shared tasks tailored to real-life contexts (e.g., community shopping, cooking, or environmental organization). A designated care staff member is responsible for facilitation, assistance, and documentation.

The intervention is conducted 2 to 3 days per week, with multiple short activity sessions per day, each lasting approximately 5 to 60 minutes, over a period of 12 weeks, with a total intervention time of approximately 1,000 minutes.

Comparatore attivo: Exercise intervention

The Vivifrail exercise program was adopted, an evidence-based intervention model for older adults developed based on international research (Izquierdo, 2019). Through graded, structured exercise training, the program aims to improve lower-limb muscle strength, balance, and gait function. In this study, it was used as a standardized exercise intervention for comparison with the reablement intervention.

The program was delivered in small groups (5-10 participants per group), led by designated care staff. Each participant received exercise training corresponding to their functional level. The intervention was conducted 2 to 3 days per week, with each session lasting 30 to 40 minutes, over a period of 12 weeks, with a total intervention time of approximately 1,000 minutes.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mobility
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Short Physical Performance Battery. It comprises three tests-balance, 4-meter walk, and chair stands-with scores ranging from 0-12, where lower scores indicate higher disability and frailty.
From enrollment to the end of treatment at 12 weeks
Fear of fall
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Short Falls Efficacy Scale International. It is a 7-item questionnaire where individuals are instructed to score their concern of falling during an activity on a 4-point Likert scale. Scores range from 7-28, where higher scores indicate higher level of fear of falling.
From enrollment to the end of treatment at 12 weeks
Number and severity of falls
Lasso di tempo: From enrollment to the end of treatment at 12 weeks, every week.
The Fall Record Form is used to document the frequency, location, and severity of the fall incident, and to provide additional details in the remarks section, including any injuries sustained and subsequent management or interventions.
From enrollment to the end of treatment at 12 weeks, every week.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Activities of daily living
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Barthel Index It is one of the most commonly used clinical tools for evaluating activities of daily living (ADL). It has a total score of 100, with lower scores indicating poorer self-care ability and a higher level of dependence on others.
From enrollment to the end of treatment at 12 weeks
Activities of Daily Living
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Lawton IADL Scale. It is an 8-item assessment tool to measure an older adult's ability to perform complex daily tasks necessary for community living. It rates independence in areas like finances, transportation, and medication management, with higher scores (0-8) indicating greater autonomy.
From enrollment to the end of treatment at 12 weeks
Activities of Daily Living
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Individualized Activity Goal Performance Scale. It is a simplified adaptation grounded in Canadian Occupational Performance Measure (COPM). Participants engage in a structured interview to select meaningful activities from common day care center tasks and may also add other personally relevant goals. For each selected activity, participants rate their perceived performance on a scale from 1 to 10 (1 = unable to perform at all; 10 = performs very well). The overall score is then calculated by averaging the ratings across all selected activities.
From enrollment to the end of treatment at 12 weeks
Well-being
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Chinese Happiness Inventory. It is based on the Oxford Happiness Inventory, developed by Lu Luo incorporated culturally specific sources of well-being relevant to Chinese populations. It adopts a 4-point Likert scale scoring system, with response options ranging from 0 to 3 and a total score range of 0 to 30. Higher scores indicate a greater level of subjective well-being. Considering older adults' language comprehension and life context, items originally categorized under the "work achievement" dimension were modified to reflect a broader "sense of accomplishment in daily life," thereby enhancing applicability and interpretability for the target population.
From enrollment to the end of treatment at 12 weeks

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 (Effettivo)

4 dicembre 2025

Completamento primario (Effettivo)

25 marzo 2026

Completamento dello studio (Stimato)

31 dicembre 2026

Date di iscrizione allo studio

Primo inviato

16 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

23 aprile 2026

Primo Inserito (Effettivo)

30 aprile 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 aprile 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

23 aprile 2026

Ultimo verificato

1 novembre 2025

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 202510081RINE

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 .

Prove cliniche su Reablement

Sottoscrivi