Informazioni generali
  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Zurigo
    (BASEC)
  • Responsabile dello studio Prof. Dr. med., DrPH Heike Annette Bischoff-Ferrari heikea.bischoff-ferrari@uzh.ch (BASEC)
  • Fonte dati BASEC: Importato da 24.06.2025 ICTRP: N/A
  • Ultimo aggiornamento 24.06.2025 12:05
HumRes66593 | SNCTP000006330 | BASEC2024-02382

ICOPE – Pilot Study

  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Zurigo
    (BASEC)
  • Responsabile dello studio Prof. Dr. med., DrPH Heike Annette Bischoff-Ferrari heikea.bischoff-ferrari@uzh.ch (BASEC)
  • Fonte dati BASEC: Importato da 24.06.2025 ICTRP: N/A
  • Ultimo aggiornamento 24.06.2025 12:05

Descrizione riassuntiva dello studio

In 2015, the WHO published a report outlining six key functions that people value most: mobility, cognition, mental health, vision, hearing, and nutrition/vitality. Since a decline in one or more of these functions leads to reduced health and quality of life, the WHO developed the 'Integrated Care for Older People' (ICOPE) program to prevent and improve these functions. The goal is to conduct a large study (800 men and women in Switzerland). To assess feasibility within the structures of Switzerland, we are conducting a pilot study ICOPE-Pilot with 100 people in collaboration with Pro Senectute Kanton Zürich (PS ZH). Participants must be 70 years or older, live independently at home, and be mobile enough to visit the service centers of PS ZH. Additionally, there must be an impairment in at least 2 of the ICOPE functions. Participants will be randomly assigned to two groups: the 'intervention group' and the 'control group'. The intervention group will be supported by the ICOPE nurse (4 visits/calls and a hotline) and will receive a tailored multi-component program. For example, this program for a mobility limitation would not only offer various exercise programs to strengthen muscles but also provide dietary recommendations or strategies to promote social interactions, or adjustments to medications that may cause falls, depending on the person's needs. At the same time, participants in the intervention group will also receive guidance to strengthen the functions that are not yet impaired. The control group will receive no intervention. All participants are scheduled for 2 study visits (start, after 6 months) at the Center for Aging and Mobility (ZAM), as well as a follow-up phone call (after 12 months).

(BASEC)

Intervento studiato

The ICOPE interventions are based on the WHO's ICOPE manual. They are tailored individually and personally to the study participants and include the prevention of deterioration in impaired functions, as well as the strengthening of non-impaired functions. The 6 functions focused on by ICOPE are mobility, cognition, mental health, vision, hearing, and nutrition/vitality. The intervention programs are co-designed with a specially trained ICOPE nurse and the study participants. They are based on recommendations formulated by international experts, are evidence-based, and consider benefits, costs, resource use, and the values of older adults in a balanced manner. The individual interventions are selected to best meet the participants' needs (personalization) and to be as accessible as possible. The intervention will be conducted and planned in five community centers of Pro Senectute Kanton Zürich in the canton of Zurich (Winterthur, Bülach, Horgen, Wetzikon, and the city of Zurich). Additionally, a hotline will be established, through which participants in the intervention group can discuss and seek advice from the ICOPE nurse at any time.

(BASEC)

Malattie studiate

Pilot study for individual, personalized, and integrated prevention and strengthening of the 6 ICOPE functions: mobility, cognition, mental health, vision, hearing, and nutrition/vitality.

(BASEC)

Criteri di partecipazione
- Women and men aged 70 years or older - Living independently in the community (own or rented house/apartment, senior housing). - Currently existing impairment in at least two of the six ICOPE functions. This will be assessed in two steps: (1) an online questionnaire (conducted independently or with the help of staff from Pro Senectute Kanton Zürich), and (2) a telephone screening for general study eligibility and verification of the pre-screening regarding the ICOPE functions, conducted by the study team at the Center for Aging and Mobility (ZAM). (BASEC)

Criteri di esclusione
- Predominant severe cognitive impairment/dementia (Baseline Mini Mental State Examination of < 24). - Severe mobility, hearing, vision, or speech impairment. - Acute medical condition at the start of the study or severe medical condition with an expected survival time of less than 1 year. (BASEC)

Luogo dello studio

Zurigo

(BASEC)

non disponibile

Sponsor

University Department of Geriatric Medicine FELIX PLATTER (UAFP) Prof. Reto W. Kressig

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Prof. Dr. med., DrPH Heike Annette Bischoff-Ferrari

+41 044 417 22 17

heikea.bischoff-ferrari@uzh.ch

Zentrum Alter und Mobilität

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione etica Zurigo

(BASEC)

Data di approvazione del comitato etico

18.03.2025

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
ICOPE–Function-Centered & Person-Centered Health Promotion Trial for Adults 70+: a 6-month randomized controlled pilot trial with a follow-up at 12 months to record sustainability of benefits (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile