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Determinants of Patients' Uptake of Therapeutic Education Programme

Determinants of Patients' Uptake of Therapeutic Education Programme

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03255863
Acronym
UTEP
Enrollment
459
Registered
2017-08-21
Start date
2017-12-20
Completion date
2020-09-09
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Disease, Empathy, Patient Adherence, Patient Education as Topic, Quality of Healthcare

Keywords

Psychological Theory

Brief summary

Therapeutic Patient Education (TPE) refers to programs that help patients to manage life with a chronic disease in the best possible way. In spite of the effectiveness of Therapeutic Patient Education, few patients uptake TPE when it is proposed to them. Therefore, our main aim was to identify patients' beliefs that will predict patients' uptake of TPE. According to the Health Belief Model, patient will participate in TPE if they perceive their disease as a serious threat (with possible serious complications), but which can be controlled however, and that TPE is efficient and represents little burden. Secondary aims are as follows: 1. To test whether the way TPE is presented to patients impact patients' decision to uptake TPE. The way TPE is presented comprises the time between diagnosis and the proposal of TPE, whether patient is a remission or crisis period in the disease, the time between the proposal and the next TPE session, and what is said by healthcare professionals to present TPE. 2. To test whether healthcare professionals' empathy impact patients' decision to participate in TPE 3. To test whether patients' intention to participate in TPE will predict their actual participation. The ultimate goal of the study is to identify patients whose beliefs will not favor participation in TPE in order to accompany those patients more carefully. Best practices will be proposed according the results.

Interventions

OTHERQuestionnaire

Patient Self reported questionnaire filled in.

Sponsors

Ministry of Health, France
CollaboratorOTHER_GOV
University Hospital, Lille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients to whom TPE was proposed in diabetes, hemophilia, obesity, cardiac failure, chronic inflammatory bowel disease, parkinson, rare diseases, epilepsy, peripheral arterial diseases * Belong to a social security scheme * Pregnant women to whom TPE for gestational diabetes is proposed

Exclusion criteria

* Cognitive impairment declared by healthcare professionals * Inpatients * Patients for whom TPE is coupled with rehabilitation * Psychiatric disorders * Patients who cannot give informed consent * Patients in jail

Design outcomes

Primary

MeasureTime frameDescription
Patient's intention to participated in TPE by a questionnaire based on the Health Belief ModelBaseline (after TPE proposal)Patient's participation in TPE : yes or no Participation is defined as the patient's intention to come expressly to the hospital for a first appointment dedicated to therapeutic education. The main variables of the HBM will be analyzed: perceived threat of the pathology, perceived benefits and barriers to TPE, perceived patient control of its pathology.

Secondary

MeasureTime frameDescription
Time limit of first proposition in TPEBaselineTime between date of diagnostic illness and date of first first proposition in TPE
Timeout of first participation in TPEBaselineTime between date of proposition and date of the program begin of TPE
Medical context in which TPE is proposedBaselineMedical context in acute phase versus phase of stabilization of the pathology
Consultation And Relational Empathy (CARE) questionnaireBaselineThe patient's perceived empathy of the professional (s) who offered the TPE will be assessed by the CARE questionnaire
Visual analog scale for intention to participatedBaselineVisual analog scale ranging from 0 not at all intending to participate to 100 very strong intention to participate Measurement of the patient's intention to participate in the proposed TPE program

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026