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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05831384
Other study ID # APHP230419
Secondary ID 2023-A00342-43
Status Completed
Phase
First received
Last updated
Start date May 11, 2023
Est. completion date May 30, 2023

Study information

Verified date August 2023
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective is to assess the overall diabetes distress score in adult patients with diabetes during their hospitalization in a diabetes ward, using the Diabetes Distress Scale (DDS-17). The correlation between the overall diabetes distress score and the patient's glycosylated haemoglobin will then be assessed.


Description:

The health consequences of emotional problems are associated with poor self-care behaviour, poor metabolic outcomes (HbA1c) and reduced quality of life. If quarterly glycated haemoglobin (HbA1c) testing is the gold standard for monitoring the risk of diabetes complications, should it not be systematically combined with the assessment of distress related to living with diabetes? To our knowledge, there are few studies in France that have correlated glycaemic control with a scale assessing the emotional stress factors associated with diabetes. The main objective is to evaluate diabetes-related distress in adult patients with diabetes during their hospitalization in a diabetes ward, using a self-assessment instrument: the Diabetes Distress Scale (DDS-17). The secondary objective is to assess the correlation between the overall diabetes distress score and the patient's glycosylated haemoglobin.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date May 30, 2023
Est. primary completion date May 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients living with type 1 or type 2 diabetes. - Patients hospitalised in the diabetes department of the IE3M. - Patients aged ? 18 years. - Patients agreeing to participate in this study after information. - Beneficiary of the health insurance. Exclusion Criteria: - Refusal to participate. - Inability to communicate in French. - Inability to read or write French. - Communication disorders. - History of psychiatric disorders, dementia. - Patient under guardianship or curatorship. - Patient not affiliated to social security. - Patient affiliated to the Aide Médicale d'Etat (AME).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Diabetology department - Hospital of Pitié Salpêtrière - APHP Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall diabetes distress score The primary endpoint is the overall diabetes distress score obtained by the DDS-17 psychometric tool. Each item is rated on a 6-point scale ranging from (1) "not a problem" to (6) "a very significant problem".
Each of the 17 criteria of the DDS17 is rated on a 6-point scale ranging from (1) "not a problem" to (6) "a very important problem".
The scale gives an overall distress score based on the average responses on the 1-6 scale for the 17 items.
Interpretation of the DDS 17 total scores:
Mean score < 2.0 = reflects little or no distress
Mean score between 2.0 and 2.9 = reflects moderate distress
Mean score > 3.0 = reflects high distress.
at baseline
Secondary The The patient's glycated haemoglobin (Hba1c) result, expressed as a %, taken during the standard check-up on the day of admission to hospital result (Hba1c) The patient's glycated haemoglobin (Hba1c) result, expressed as a %, taken during the standard check-up on the day of admission to hospital. at baseline
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