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Clinical Trials/NCT04197258
NCT04197258
Recruiting
Not Applicable

Evaluation of the Impact of an Individual Peer Support Intervention for Stroke Patients When Returning Home: a Mixed Methods Pilot Study

Hospices Civils de Lyon1 site in 1 country40 target enrollmentOctober 9, 2020
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Hospices Civils de Lyon
Enrollment
40
Locations
1
Primary Endpoint
Feasibility measure
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

Going back home following a stroke is a key step for the patient and his or her relatives. Due to the brutality of stroke and increasingly shorter in-hospital lengths of stay, patients and their families must adapt quickly to the patient's new health functioning and the new caregiving and support role for family members.

Peer support could be an innovative and inexpensive approach to addressing these issues. Peer-helpers are patient-partners who put their experiential knowledge from life with the disease at the disposal of other patients to offer them social and emotional support in the management of the disease in connection with care, social and community structures. Group peer support programs face organizational challenges and fail to address the full range of patient needs for stroke home visits. Individualized and more flexible support could better meet the needs of patients. Our hypothesis is that individual peer support improves quality of life and patient empowerment during the discharge period compared to usual practice.

Registry
clinicaltrials.gov
Start Date
October 9, 2020
End Date
December 5, 2026
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patient,
  • Having had a first confirmed, ischemic or hemorrhagic stroke
  • Managed in the participating rehabilitation center
  • Whose discharge to home directly from the rehabilitation center is planned
  • Presenting a modified Rankin score of 1 to 3 when deciding to leave the stroke center
  • Having given its written consent
  • Whose main residence is located in the Rhône department
  • Aphasic patients may be included if a caregiver can follow up with the case manager

Exclusion Criteria

  • Patient living in an institution prior to stroke
  • included in a gerontological network before stroke
  • Patient unable to understand quality of life questionnaires
  • Patient with unstable medical or psychological conditions who, in the opinion of the investigator, could lead the subject to be non-compliant or uncooperative during the study or could compromise patient safety or participation in the study
  • Patient under guardianship or curatorship
  • Patient not affiliated to a social health insurance

Outcomes

Primary Outcomes

Feasibility measure

Time Frame: 6 months

The feasibility of the intervention will be evaluated as success with a combined criteria including: * Recruitment and training of 2 peer helpers, * Support offered to 20 patients by the peer helpers during the intervention period defined by at least one meeting before and one contact after discharge per patient included in period after, * Good acceptability by patients, carers and peer helpers. These data will be collected by a qualitative approach associating semi-directive interviews, focus groups and participant observation.

Secondary Outcomes

  • Disability(6 months)
  • Adherence(6 months)
  • Human, material and financial assistance provided at home(6 months)
  • Quality of life between the discharge from hospital and 6 months(6 months)
  • Anxiety and depression scores between discharge and 6 months(6 months)
  • Patient activation Measure(6 months)
  • Satisfaction measure(6 months)
  • Caregiver burden(6 months)
  • Caregiver satisfaction(6 months)

Study Sites (1)

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