METIS: Impact of a Training in Therapeutic Education on the Relation Between Care Givers and Their Patients

• Sponsor: Centre Hospitalier Universitaire de Besancon (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT03323996
• Collaborator: (none)
• Enrollment: 40
• Location: 1
• Anticipated Duration (Months): 16.2
• Patients Per Site Per Month: 2.5

Study Details

Study Description

Brief Summary

This study aims to describe the impact of a training in therapeutic education on the relation between a caregiver and his/her patients.

Subjects are recruited among health professionals attending a training in therapeutic education. Then they are asked to identify up to 5 of their patients to be contacted by the researcher for an interview.

Individual semi-structured interviews are conducted with 20 duo "caregivers / patients" before the training, 1 month and 6 months after the training.

Condition or Disease	Intervention/Treatment	Phase
Cancer of Liver; Diabetes	Other: Semi-Structured interviews

Study Design

• Study Type: Observational
• Anticipated Enrollment: 40 participants
• Observational Model: Other
• Time Perspective: Prospective
• Official Title: Impact of a Training in Therapeutic Education on the Relation Between Care Givers and Their Patients
• Actual Study Start Date: Jul 26, 2017
• Anticipated Primary Completion Date: Sep 1, 2018
• Anticipated Study Completion Date: Dec 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
Health Professionals Health Professionals attending a training in therapeutic education	Other: Semi-Structured interviews; individual semi-structured interviews
Patients Patients of the health Professionals recruited for the study	Other: Semi-Structured interviews; individual semi-structured interviews

Outcome Measures

Primary Outcome Measures

1. Semi-Structured interviews [9 months]

   Qualitative analysis - theorical saturation

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Informed consent to participate to 3 interviews

Exclusion Criteria:

• Not fluent French speaker

• Patient under guardianship

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	CHU de Besançon	Besançon		France	25000

Sponsors and Collaborators

• Centre Hospitalier Universitaire de Besancon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Centre Hospitalier Universitaire de Besancon
• ClinicalTrials.gov Identifier: NCT03323996
• Other Study ID Numbers: P/2016/307
• First Posted: Oct 27, 2017
• Last Update Posted: Oct 27, 2017
• Last Verified: Oct 1, 2017

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Liver Neoplasms

Study Results

No Results Posted as of Oct 27, 2017