Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Psychological Distress and Type 2 Diabetes (COPEST)

17 januari 2020 bijgewerkt door: Azienda Ospedaliera Universitaria Integrata Verona

Glycaemic Control, Body Weight and Psychological Distress in Type 2 Diabetes: The Role of Self-Efficacy

Increasing evidence suggests that psychological disorders play an important role in the development and worsening of type 2 diabetes (T2D). Among the spectrum of psychological disorders, there is a wide literature about the association between depression and T2D and current data show an approximately two-fold prevalence of depression in adults affected by diabetes compared to un-affected subjects. Moreover, depression in diabetic patients is associated with higher blood glucose levels, poorer adherence to therapeutic regimens (whether pharmacological or therapeutic lifestyle changes), more medical complications, and higher hospitalization rates. Nevertheless, at the best of our knowledge, the mechanism underlying the association between depression and adverse diabetes-related outcomes is currently unresolved.

Aim of this project is to assess the efficacy of a psychological treatment for diabetic patients with suboptimal level of Hemoglobin A1c. This project is a RCT that seeks to address the question if type 2 diabetic patients with suboptimal glycaemic control would benefit from a specific psychological intervention, as specified below. A total of 80 diabetic patients will be recruited and randomly assigned to two treatment arms:

  1. Standard diabetes care
  2. 24 individual sessions of psychological intervention The expected main outcome is the improvement of glycaemic control under psychological intervention in 38 weeks of follow up.

Secondary outcomes: reduction of depression and anxiety, improvement in self-efficacy, perceived interference caused by diabetes, family support and eating problems.

Studie Overzicht

Toestand

Geschorst

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

Several studies have reported higher level of psychological disorders in people with diabetes such as depression and anxiety. A recent meta-analysis suggests that the odds of depression in the diabetic patients is twice than in nondiabetic subjects and this difference persists even after adjustment for sex, type of diabetes or assessment method. Furthermore, depression is significantly associated with hyperglycemia. Several proposals exist to explain this association.

The aim of this project is to study the effect of a psychological intervention based on cognitive-behavioural strategies in patients with type II diabetes. The effect will be evaluate on both physiological and psychosocial parameters. The hypothesis is that a psychological intervention based on cognitive behavioural strategies increases patient's belief in his self-efficacy to succeed in diabetes care. The improvement in self-efficacy will therefore lead to improve the psychological status, i.e. depression.

Material and Methods: The investigators will perform a randomized controlled trial (RCT). A sample of 80 type 2 diabetic patients will be recruited at Endocrinology Unit of Verona Hospital during routine medical examination and then randomly assigned to intervention or control arm. In details, patients will be first recruited for participation in the study by their physician. Thereafter, patients will be approached by psychologist who will explain research and its goals. Control group will receive current standard of diabetes care. Intervention group will receive a weekly psychological intervention based on cognitive behavioural strategies. Each session will be based on self-monitoring, problem solving and goal setting. The first session will be held two weeks after the enrollment and the last one will take place at twenty-sixth week. Subjects will be given a food and physical activity diary as well as a pedometer. Study participants will weekly fill in the diary starting from 2nd session until the 19th session for a total of 18 weeks. Subjects will carry the pedometer for the same time window.

The psychological intervention comprises three phases:

PHASE 1 (1°-2° session):

  • Psychological testing
  • Therapeutic alliance formation
  • Goal definition

PHASE 2 (3°-19°)

  • Food and physical activity self-monitoring
  • Identifying unhealthy behaviours and helping subject to change them
  • Identifying negative beliefs and replace them with positive and healthy ones
  • Providing coping strategies to stress and emotions

PHASE 3 (20°-24°)

  • Reinforcing behaviour modification
  • Identifying possible barriers
  • Activation of personal and social resources

Outcome measures will be assessed at baseline (pre-treatment), after 26 weeks treatment (post-treatment) and at 38 weeks follow up (follow-up).

Studietype

Ingrijpend

Inschrijving (Werkelijk)

61

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • Italië
      • Verona, Italië, 37126
        • Division of Endocrinology and Metabolic Diseases

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

25 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Type 2 diabetes diagnosed at least 1 year before enrollment
  • 25 ≤ BMI ≤ 40 Kg⋅m-2
  • 25 to 75 years
  • HbA1c > 7,0%

Exclusion Criteria:

  • Current schizophrenia/ psychotic disorders, bipolar disorders, addictive disorders, personality disorders
  • Current psychotherapy
  • Severe physical illness (i.e. cancer)
  • Pregnancy
  • Eligibility to bariatric surgery

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Psychological Intervention
Cognitive Behavioural Intervention
Gedragsmatig: Cognitive-Behavioral Intervention

1 weekly individual 45 min-session for 24 weeks. The program comprises the following cognitive-behavioral strategies:

  • self-monitoring
  • problem solving
  • goal definition
  • cognitive restructuring
  • activation of personal and social resources
Geen tussenkomst: Current standard of care

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline glycosylated haemoglobin (HbA1c) at 26th and 38th weeks [mmol/mol]
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)
Glycosylated haemoglobin (HbA1c) is a lab test that shows the average level of blood glucose over the previous 3 months. HbA1c is used in the present study as measure of the glycaemic control: it will be assessed at baseline (pre-treatment), after 26 weeks treatment (post-treatment) and at 38 weeks follow up (follow-up).
Baseline, 26 weeks (post-treatment)-38 weeks (FU)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline Body Mass Index (BMI)at 26th and 38th weeks [Kg/m2]
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Body Mass Index is a measure of adiposity and is used here as anthropometric marker of life style change.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline depressive symptoms at 26th and 38th weeks (BDI-II score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]

The Beck Depression Inventory II is a 21-item questionnaire developed to assess the intensity of depression as defined by the Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition (DSM-IV). The BDI-II items include (1) cognitive symptoms such as sadness and pessimism, (2) affective symptoms such as loss of pleasure and loss of interest, (3) somatic symptoms such as loss of energy, appetite changes and changes in sleep pattern.

The BDI-II is calculated by summing the ratings for the 21 items. The 4-point scale ranges from 0 to 3 for each item. The maximum total score is 63.

The measurement of outcome variables will be conducted 38 weeks after termination of the treatment (38 weeks follow up). The difference of the BDI-II scores among baseline (pretreatment), at the end of the 26 weeks treatment (post-treatment), and at 38 weeks follow up (follow-up) will be also calculated.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline anxiety symptoms at 26th and 38th weeks(BAI score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]

The Beck Anxiety Inventory is a 21- item questionnaire developed to assess the severity of an anxiety in adult and adolescents. The items in the BAI describe the emotional, physiological and cognitive symptoms of anxiety.

The 4-point scale ranges from 0 to 3 for each item. The maximum total score is 63.

The decisive measurement of the outcome variables will be conducted 38 weeks after termination of the treatment (38 weeks follow up). The difference of the BDI-II scores among baseline (pretreatment), at the end of the 26 weeks treatment (post-treatment), and at 38 weeks follow up (follow-up) will be also calculated.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline general perceptions of diabetes at 26th and 38th weeks (MDQ Section 1 score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]

The Multidimensional Diabetes Questionnaire (MDQ) was designed to provide a comprehensive assessment of diabetes-related cognitive and social factors. It includes 41 items subcategorized in three sections. The first section assesses the general perceptions of diabetes and related social support. It is comprised of three scales. These scales targets:

  1. perceived interference caused by diabetes to daily activities, work and social activities (9 items);
  2. perceived severity of diabetes ( 3 items);
  3. perceived diabetes-related social support from a significant other such as family, friends and health professionals (4 items).

Responses were rated on 7-point rating scales (from 0 to 6), with higher scores indicating higher levels of perceived interference, social support and severity.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline family support at 26th and 38th weeks (MDQ section II score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
This section of the MDQ measures social incentives in relation to self-care activities. The scales included in this section were designed to measure the frequency of positive reinforcing behaviour (8 items) and the frequency of non supportive behaviours (4 items). Subjects recorded their responses on 7-point Likert scales (from 0 to 6) with higher scores indicating higher levels of positive and negative reinforcement behaviours.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline Diabetes Self-Efficacy at 26th and 38th weeks (MDQ section III score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
This section of the MDQ is used to assess self-efficacy expectancies (7 items) and outcome expectancies (6 items). The self-efficacy scale measured patients' confidence in their ability to perform behaviours specific to the diabetes self-care activities. Responses were rated on a 0 to 100 rating scale. The outcome expectancies scale assessed patients' perceptions of the effect of diabetes self-care behaviours on metabolic control. Responses were rated on a 0 to 100 rating scale.
Baseline, 26 weeks (post-treatment)-38 weeks (FU)]
Change from baseline Binge-Eating Disorders at 26th and 38th weeks (BES score)
Tijdsspanne: Baseline, 26 weeks (post-treatment)-38 weeks (FU)

The Binge-Eating Scale (BES) is a 16-item questionnaire developed to assess the presence of binge eating behaviour indicative of eating disorders. The BES includes questions on subjects' concerns about weight and food, inability to control urges to eat, feelings of guilt after eating and frequency of strict dieting.

Each question has 3-4 separate responses assigned a numerical value. The score ranges is from 0-46
Baseline, 26 weeks (post-treatment)-38 weeks (FU)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Azienda Ospedaliera Universitaria Integrata Verona

Onderzoekers

  • Hoofdonderzoeker: Enzo Bonora, MD, Universita di Verona

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 oktober 2012

Primaire voltooiing (Werkelijk)

1 maart 2015

Studieregistratiedata

Eerst ingediend

19 april 2013

Eerst ingediend dat voldeed aan de QC-criteria

3 juni 2013

Eerst geplaatst (Schatting)

5 juni 2013

Updates van studierecords

Laatste update geplaatst (Werkelijk)

22 januari 2020

Laatste update ingediend die voldeed aan QC-criteria

17 januari 2020

Laatst geverifieerd

1 januari 2020

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • CE-2212 Ago, 29 2012

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Klinische onderzoeken op Type 2 diabetes

Klinische onderzoeken op Cognitive-Behavioral Intervention

Zoek naar vergelijkbare onderzoeken

Sponsors en medewerkers

Medische omstandigheden

Geneesmiddelinterventies

CROs by country

CROs in Morocco

Voorwaarden

Zeldzame ziekten

Geneesmiddelinterventies

Voedingssupplementen

Sponsor / medewerkers

Locaties

Abonneren