Effect of Personalised Citizen Assistance for Social Participation(APIC) on Older Adults Health and Social Participation

NCT ID: NCT03161860

Last Updated: 2025-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

180 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-04

Study Completion Date

2025-12-31

Brief Summary

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Global aging and the growing burden of chronic diseases represent a challenge. Innovative interventions acting upon health determinants, like social participation, are required. Social participation, defined as the involvement of a person in activities that provide interactions with others in the community is critical to promote health and prevent disabilities. Many older adults do not have equitable opportunities to achieve full social participation, and interventions under-empower their personal and environmental resources and only reach a minority. To optimize current practices, the Personalised citizen assistance for social participation (APIC), an intervention demonstrated as being feasible and having positive impacts, needs further evaluation.

The first aim of this study is evaluate the impacts of the APIC on older adults' health, social participation, life satisfaction and healthcare services utilisation. The second aim is to evaluate the cost-effectiveness of the intervention. In parallel, the implementation of the APIC, including factors facilitating and impeding it, will be documented.

Concerning the first two objectives, two hypotheses are formulated: 1) the APIC will prevent a decline in older women's and men's health, social participation and life satisfaction, and reduce their use of healthcare services, and 2) the APIC will be associated with lower costs, from older adults', healthcare system and societal perspectives, including healthcare expenditures.

Detailed Description

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Conditions

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Community-dwelling Older Adults

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors
Due to the type of intervention, coordinators, volunteers and participants will not be blinded to the interventions. However, they will not be informed about the study hypotheses. Research assistants and the statistician responsible for the analysis will be blinded to the intervention until completion of the study.

Study Groups

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Personalised citizen assistance

The experimental group will receive the Personalised citizen assistance for social participation (APIC), i.e. weekly 3-hour personalised stimulation sessions by a trained volunteer over 12 months. Sessions will encourage empowerment, gradual mobilisation of personal and environmental resources, and community integration.

Group Type EXPERIMENTAL

Personalised citizen assistance for social participation(APIC)

Intervention Type BEHAVIORAL

The APIC involves a non-professional attendant who, after 2 to 5 days of training, provides a two to three-hour stimulation session each week over a six to eighteen-month period targeting significant social and leisure activities that are otherwise difficult for older adults to accomplish.

Control group

The control group will receive the publicly-funded universal healthcare services available to all Quebecers.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Personalised citizen assistance for social participation(APIC)

The APIC involves a non-professional attendant who, after 2 to 5 days of training, provides a two to three-hour stimulation session each week over a six to eighteen-month period targeting significant social and leisure activities that are otherwise difficult for older adults to accomplish.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. be aged 65 or older,
2. live at home or in seniors' residences,
3. be restricted in at least one instrumental activity of daily living (e.g. house cleaning, shopping), and
4. have a good understanding of French or English.

Exclusion Criteria

* Moderate to severe cognitive impairments
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Canadian Institutes of Health Research (CIHR)

OTHER_GOV

Sponsor Role collaborator

Mélanie Levasseur

OTHER

Sponsor Role lead

Responsible Party

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Mélanie Levasseur

Research Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Mélanie Levasseur

Role: PRINCIPAL_INVESTIGATOR

Université de Sherbrooke; Research centre on aging

Locations

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Centre d'action bénévole Drummond

Drummondville, Quebec, Canada

Site Status

Centre d'action bénévole Bellechasse-Lévis-Lotbinière

Lévis, Quebec, Canada

Site Status

Service d'aide et de référencement Anjou (SARA-Anjou)

Montreal, Quebec, Canada

Site Status

Carrefour communautaire Montrose

Montreal, Quebec, Canada

Site Status

Centre ABC

Montreal, Quebec, Canada

Site Status

Accorderie de Sherbrooke, coopérative de solidarité

Sherbrooke, Quebec, Canada

Site Status

Countries

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Canada

References

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Levasseur M, Chaintre-Prieur A, Dubois MF, Maisonneuve C, Filiatrault J, Vassiliadis HM. Strengths, challenges, and strategies for implementing pragmatic multicenter randomized controlled trials (RCTs): example of the Personalized Citizen Assistance for Social Participation (APIC) trial. Trials. 2024 Jun 27;25(1):415. doi: 10.1186/s13063-024-08248-w.

Reference Type DERIVED
PMID: 38937798 (View on PubMed)

Levasseur M, Dubois MF, Filliatrault J, Vasiliadis HM, Lacasse-Bedard J, Tourigny A, Levert MJ, Gabaude C, Lefebvre H, Berger V, Eymard C. Effect of personalised citizen assistance for social participation (APIC) on older adults' health and social participation: study protocol for a pragmatic multicentre randomised controlled trial (RCT). BMJ Open. 2018 Mar 31;8(3):e018676. doi: 10.1136/bmjopen-2017-018676.

Reference Type DERIVED
PMID: 29605819 (View on PubMed)

Other Identifiers

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MP-31-2018-2424

Identifier Type: -

Identifier Source: org_study_id

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