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Cohort Study of Patients With Type 1 Diabetes

2. juli 2022 oppdatert av: Zhiguang Zhou, Second Xiangya Hospital of Central South University

Cohort Study of Patients With Type 1 Diabetes:Clarifing the Underlying Hereditary and Autoimmune Pathogenic Factors

This study aims to clarify the underlying hereditary and autoimmune factors that contribute to clinical type 1 diabetes and gain a better understanding of the natural history of the disease.

Studieoversikt

Studietype

Observasjonsmessig

Registrering (Faktiske)

2110

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Hunan
      • Changsha, Hunan, Kina, 410011
        • Institute of Metabolism and Endocrinology, Second Xiangya Hospital, Central South University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

type 1 diabetes patients

Beskrivelse

Inclusion Criteria:

  1. diabetes diagnosed according to the report of WHO (World Health Organization) in 1999;
  2. insulin dependence from disease onset,thus diagnosed with type 1 diabetes;
  3. all patients gave informed consent to participate in the study and the protocol was approved by the Research Ethics Committee in second Xiangya hospital, Central South University.

Exclusion Criteria:

  1. secondary diabetes mellitus;
  2. pregnant women;
  3. malignant disease.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Intensive structured education group
Regular outpatient visit in every 3 months to these patients. The glucose control and diabetes complication screening will be evaluated in visit. Patients will also be evaluated by specialized psychologists, dietitians and therapists. Diabetes self-management education will be regularly exposed to patients
The structured education is based on a regular outpatients visit.It is an education that integrated several diabetes related subjects,which mainly aimed at T1D self-management.
Conventional education group
Outpatients visit to endocrinologists when necessary in a conventional way.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Effects of structured education on β-cell endocrine function progression of T1D patients.
Tidsramme: Baseline and every three months afterwards.

The natural progression of patients' β-cell endocrine functions was assessed by fasting C-peptide (FCP) and postprandial C-peptide (PCP) at each visit. FCP and PCP levels were measured at initial recruitment and every three months after that. The decay rate of β-cell endocrine function of patients in the two groups were compared.

Serum C-peptide levels were measured by a chemiluminescence method using a commercial available kit (Adiva Centaur System, Siemens, Germany).

Baseline and every three months afterwards.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Effects of structured education on blood sugar control.
Tidsramme: Baseline and every three months afterwards.
Patients' daily insulin dosage (U/Day) were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.
Baseline and every three months afterwards.
Effects of structured education on blood sugar control.
Tidsramme: Baseline and every three months afterwards.
Patients' blood sugar levels were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.
Baseline and every three months afterwards.
Effects of structured education on blood sugar control.
Tidsramme: Baseline and every three months afterwards.
Patients' HbA1c levels were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.HbA1c concentration was tested by the Bio-Red Variant automatic measurement system.
Baseline and every three months afterwards.
Effects of structured education on metabolic control.
Tidsramme: Baseline and every three months afterwards.
Patients' body mass index (BMI) levels were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.
Baseline and every three months afterwards.
Effects of structured education on metabolic control.
Tidsramme: Baseline and every three months afterwards.
Patients' systolic blood pressure (SBP) and diastolic blood pressure (DBP) levels were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.
Baseline and every three months afterwards.
Effects of structured education on metabolic control.
Tidsramme: Baseline and every three months afterwards.
Patients' triglyceride (TG) and total cholesterol (TC) levels were collected at initial recruitment and each visit afterwards. And the above mentioned parameters in group 1(patients with structured education) and group2(patients without structured education) were compared.
Baseline and every three months afterwards.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. oktober 2016

Primær fullføring (Faktiske)

31. desember 2021

Studiet fullført (Faktiske)

31. desember 2021

Datoer for studieregistrering

Først innsendt

11. mai 2018

Først innsendt som oppfylte QC-kriteriene

25. juli 2018

Først lagt ut (Faktiske)

2. august 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. juli 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

2. juli 2022

Sist bekreftet

1. juli 2022

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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