Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05795686

Evaluation of the Impact of the AVanCer Program Provided by the ARRPAC Day Center

Led by Hospices Civils de Lyon · Updated on 2024-06-26

162

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Each year in France, over 150,000 people experience strokes, a leading cause of adult disability, along with frequent head injuries causing similar lasting effects. These sudden events severely impact patients and their families physically, emotionally, socially, and financially. Advances in acute stroke treatments have improved survival, but ongoing support for patients returning home remains insufficient despite significant needs. The ARRPAC association is launching the AVanCer program, a specialized day center in Lyon, to enhance autonomy and adaptation for adults with brain injury sequelae and to support their caregivers. The AVanCer program offers therapeutic education, adapted physical activity, social and cognitive remediation, and therapeutic workshops. It aims to complement rehabilitation and recurrence prevention care by providing a space for patients and caregivers to share information and receive listening support. This interventional study evaluates the program's implementation and impact on participants and caregivers using the REAIM framework, monitoring reach, effectiveness, adoption, implementation, and maintenance. Participants will undergo assessments at enrollment, at program end (between 2 and 4 months), and six months later. Researchers will measure goal attainment, quality of life, depression and anxiety levels, autonomy, walking ability, treatment adherence, caregiver burden, and professional adoption of the program. Data collection includes questionnaires and evaluations like the 6-minute walking test and various validated scales. The study will track program sustainability and transferability over about 22 months.

CONDITIONS

Brief Title

Evaluation of the Impact of the AVanCer Program Provided by the ARRPAC Day Center

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female of legal age
  • Patient selected to start the AVanCer program at the ARRPAC center
  • Patient who agrees to participate in the assessment and has signed consent
  • Patient able to speak and understand French orally and in writing
  • Caregivers of legal age who agree to participate and have signed consent
  • Caregivers able to speak and understand French orally and in writing
  • Voluntary patients and caregivers who participated in the quantitative part
  • Partner professionals referring patients for support
  • ARRPAC professionals involved in the day care centre
Not Eligible

You will not qualify if you...

  • Pregnant women, parturient or breastfeeding mothers
  • Persons deprived of liberty by judicial or administrative decision
  • Persons under psychiatric care
  • Persons admitted to health or social establishments for non-research reasons
  • Persons under legal protection measures (guardian, curators)
  • Persons not affiliated with a social security scheme or similar

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Evaluation of the AVanCer Program

Duration - Between 2 and 4 months

Participants undergo assessment through the AVanCer program using quantitative and qualitative approaches.

1 baseline visit and 1 end-of-program visit (in-person)

Follow-up

Duration - Approximately 6 months after the program ends

Participants are monitored for outcomes and program effects after completing the AVanCer program.

1 follow-up visit (in-person)

Trial Site Locations

Total: 1 location

1

Accueil de jour ARRPAC

Bron, France, 69500

Actively Recruiting

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Research Team

J

Julie Haesebaert, MD

A

Anne Termoz

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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