- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT02010684
Mood and Diabetes Empowerment & Improvement Training (MADE-IT)
University of California, Los Angeles (UCLA)/Drew Project EXPORT: Mood and Diabetes Empowerment & Improvement Training (MADE IT)
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
The Phase I pilot recruited older Latinos from Dr. Mangione's previous study (who agreed to participate in future research) and 10 participants from a community settings. Those with low mood and poor glycemic control were offered a 12-week intervention combining cognitive behavioral therapy mood management techniques and diabetes self-care into one seamless intervention. Drs. Mangione and Miranda supervised and reviewed (through audiotapes) well-trained health educators conducting the intervention sessions. The study manuals were modified following this Phase I pilot intervention.
The final intervention manual was tested in a randomized trial in Phase II, compared the Mood and Diabetes Empowerment and Improvement Training intervention with enhanced care as usual (providing participants with a letter regarding their mood and hemoglobin (Hb)A1c with recommendations for improving care for their provider). The target population was low-income Latinos with depression and poor glycemic control. Both mood and diabetes outcomes are evaluated.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
-
California
-
Los Angeles, California, Stany Zjednoczone, 90095
- UCLA Psychr & Biobehav Sci
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Latino men and women age 50 and older
- Must speak English or Spanish
- Hb A1c greater than or equal to 8%
- Currently not taking medication for depression
- A score of 5 or greater on the Geriatric Depression Scale (GDS)
Exclusion Criteria:
- Persons who are legally blind, dialysis dependent, diagnosed with dementia, and/or with hemiparesis from a cerebral vascular accident
- Do not have sufficient hearing or cognitive function
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Brak interwencji: Wait-listed Control Group
Participants in the Wait-listed Control Group will receive augmented access and communication with a primary care provider.
The augmentation would consist of providing the participant with a letter to be shared with their primary care doctor indicating their Hb A1c level and depression score at the time of eligibility screening.
The research team will also attach a list of local mental health service providers to the letter.
The participants randomized to the wait-listed control group will also be offered access to the intervention after the trial is completed in the event that the randomized controlled trial (RCT) has significant results.
|
|
|
Eksperymentalny: Empowerment and CBT Classes
Participants will attend weekly 2-hour group Empowerment and CBT classes for 12 weeks led by two trained health educators.
Participants will learn cognitive behavioral therapy (CBT) techniques to manage their mood.
After CBT, participants will learn a diabetes education format that is grounded in empowerment theory that employs group problem solving, individualized goal setting, and personal behavioral change "experiments" designed to help patients set priorities and to become better self-managers of both diabetes and their mood.
As part of the intervention activities, group members will be advised to monitor their blood sugar levels, blood pressure, and mood on a daily basis.
|
Participants randomized to the intervention arm will receive a manual with 3 CBT modules and 1 Diabetes Empowerment module.
CBT Module 1 covers "Understanding Depression and Diabetes", Module 2 "How Thoughts Affect Your Mood and Diabetes Care", Module 3 "How Activities Affect Your Mood and Diabetes Care".
The Diabetes Empowerment Module covers topics including the following: food, exercise, medicine, diabetes and your health, social support, communication skills, and community resources.
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Change From Baseline in Hemoglobin A1c at 6 Months
Ramy czasowe: Baseline and 6 months
|
Hemoglobin A1c (HbA1c) measures glycemic control over the past three months.
HbA1c was measured by a blood draw and laboratory test.
|
Baseline and 6 months
|
|
Change From Baseline in Depression Measures at 6 Months
Ramy czasowe: Baseline and 6 months
|
The Geriatric Depression Scale (GDS) measures depression in older adults. The short form we used consists of 15 yes or no questions. The scale range is 0 to 15, where higher scores indicate greater severity of depression. The Patient Health Questionnaire-9 (PHQ-9) measures depression in patients. The questionnaire consists of 9 questions where patients self report how frequently they have depression symptoms over the past two weeks. The scale ranges is 0 to 27 where higher scores indicate greater severity of depression. |
Baseline and 6 months
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Change From Baseline in Blood Pressure at 6 Months
Ramy czasowe: Baseline and 6 months
|
Baseline and 6 months
|
|
|
Change From Baseline in Low Density Lipoprotein-C at 6 Months
Ramy czasowe: Baseline and 6 months
|
Baseline and 6 months
|
|
|
Change From Baseline in EQ-5D at 6 Months
Ramy czasowe: Baseline and 6 months
|
The EQ-5D measures general quality of life. The index score is based on 5 questions about mobility, self-care, pain, usual activities, and psychological status. The EuroQol Group provides a U.S. preference-weighted algorithm to calculate the index scores. A score of 1 indicates no problems while a score of -0.11 indicates severe problems. The scale score is based on a visual analog of a thermostat, where 0 represents worst imaginable health and 100 represents best imaginable health. Patients mark a tick for where they feel their health is on that scale. |
Baseline and 6 months
|
|
Change From Baseline in Yale Physical Activity Scale - Index Summary Score at 6 Months
Ramy czasowe: Baseline and 6 months
|
The Yale Physical Activity Scale measures physical function and activities of daily living.
Five activity indices (vigorous activity, leisurely walking, moving, standing and sitting) are calculated by multiplying the frequency of activity with the duration and a weighted factor.
The 5 indices are then summed to create an index summary.
Higher scores indicate more activity.
The minimum and maximum scores are 0 and 142.
|
Baseline and 6 months
|
|
Change From Baseline in Self-Efficacy (Diabetes Empowerment Scale) at 6 Months
Ramy czasowe: Baseline and 6 months
|
The Diabetes Empowerment Scale Short Form (DES-SF) measures diabetes-related psychosocial self-efficacy.
The questionnaire presents 8 statements on self-efficacy where participants rate how strongly they agree.
The answers are summed to create a score where higher scores indicate more empowerment.
The score range is 0 to 8.
|
Baseline and 6 months
|
Współpracownicy i badacze
Śledczy
- Główny śledczy: Jeanne Miranda, PhD, UCLA Psychr & Biobehav Sci
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- MADE-IT Study 1P20MD00148-03
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Cukrzyca typu 2
-
Assiut UniversityJeszcze nie rekrutacjaDiabtes Mellitus Type 1
-
Leiden University Medical CenterZakończonyGruczolak przysadki | Guz przysadki | Diabetes Insipidus Cranial Type | Dokrewny; NiedobórHolandia
-
Fondazione Policlinico Universitario Agostino Gemelli...Jeszcze nie rekrutacjaOtyłość | Cukrzyca typu 2 | Cukrzyca insulinoodporna (Mellitus)
-
Centre Hospitalier Universitaire de LiegeSanofi; Takeda; University of Liege; Orchard Therapeutics; Centre Hospitalier Régional... i inni współpracownicyZakończonyWrodzony przerost nadnerczy | Hemofilia A | Hemofilia B | Mukopolisacharydoza I | Mukopolisacharydoza II | Mukowiscydoza | Niedobór alfa 1-antytrypsyny | Anemia sierpowata | Anemia Fanconiego | Przewlekła choroba ziarniniakowa | Choroba Wilsona | Ciężka wrodzona neutropenia | Niedobór transkarbamylazy ornityny | Mukopolisacharydoza... i inne warunkiBelgia
-
UK Kidney AssociationRekrutacyjnyZapalenie naczyń | AL Amyloidoza | Stwardnienie guzowate | Choroba Fabry'ego | Cystynuria | Ogniskowe segmentowe stwardnienie kłębuszków nerkowych | Nefropatia IgA | Syndrom Barttera | Czysta aplazja czerwonokrwinkowa | Nefropatia błoniasta | Atypowy zespół hemolityczno-mocznicowy | Autosomalna dominująca policystyczna... i inne warunkiZjednoczone Królestwo
Badania kliniczne na Empowerment and CBT Classes
-
Charite University, Berlin, GermanyGerman Federal Ministry of Education and ResearchZakończony
-
University of LuxembourgQuresta, Inc.; National Psychological Association of Ukraine; Veteran Mental Health...RekrutacyjnyZespołu stresu pourazowego | Zespół stresu pourazowego PTSD | Zespół stresu pourazowego, PTSDUkraina