- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01901952
Lifestyle Improvement Through Food and Exercise (LIFE)Study (LIFE)
8 maj 2017 uppdaterad av: Rush University Medical Center
Lifestyle Improvement Through Food and Exercise (LIFE) Study
The primary aim of the LIFE study is to compare low-income African American diabetes patients in a lifestyle intervention group with those in a standard of care control group on change in glycemic control at 12-months.
We hypothesize that, on average, participants in the intervention group will achieve greater glycemic control at 12-months relative to their baseline A1c, than those in the control group.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This project is a randomized controlled trial to test an innovative lifestyle intervention to achieve sustained improvements in glycemic control among low-income African American diabetes patients.
The LIFE (Lifestyle Improvement through Food and Exercise) program is a diabetes self-management program focused on diet and exercise, informed by anthropological research on models of food and health among low-income African-Americans.
Pilot work demonstrated that the LIFE Program is effective in improving glycemic control among low-income African Americans at 6-months.
The main goal of the current study is to determine whether the LIFE Program can achieve sustained improvements in glycemic control for 12 months.
The trial will randomize low-income African American adults with diabetes to a control group, which receives standard diabetes education, or an intervention group, which receives the LIFE Program (28 group meetings with peer support telephone calls) followed by a 6-month maintenance phase (quarterly group sessions with monthly peer support phone calls).
The primary aim of the proposed research is to compare low-income African American diabetes patients receiving the LIFE Program with those in a standard of care control group on change in glycemic control at 12 months.
Our primary hypothesis is that patients in the intervention group will achieve a change in A1c from baseline that is less than patients in the control group.
Secondary aims are to compare low-income African American diabetes patients receiving the LIFE Program with those in a standard of care control group on (a) change in glycemic control at 18 months; (b) change in physical activity and total energy intake at 12 months; (c) change in physical activity and total energy intake at 18 months; and (d) to obtain estimates needed for a subsequent trial, including weight, blood pressure, and diabetes-related hospitalizations.
For secondary aims we hypothesize that a) the intervention group will achieve a mean 18-month change in A1C that is less than the change in the control group; b) at 12 months, a greater proportion of intervention patients will have achieved the activity goal of 150 minutes of moderate activity per week, and the intervention group will achieve a greater reduction from baseline in mean total energy intake than the control group; and c) at 18 months, a greater proportion of intervention patients will have achieved the activity goal of 150 minutes of moderate activity per week, and the intervention group will achieve a greater reduction from baseline in mean total energy intake than the control group.
Studietyp
Interventionell
Inskrivning (Faktisk)
211
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Illinois
-
Chicago, Illinois, Förenta staterna
- Cook County Health Clinics
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Diagnosis of type 2 diabetes mellitus (T2DM) and HbA1c > 7%;
- Patients must identify themselves as African American;
- Patients must be patients of Cook County Hospital ambulatory clinics;
- Primary care physician gives clearance for patient to participate in study and engage in moderate level physical activity.
Exclusion Criteria:
- BMI<18.5;
- Patient not on diabetes medication and with a HbA1c reading less than 7%
- End-stage renal disease, stroke with paresis, congestive heart failure (NYHA class 2-4), or other major end-organ complication of diabetes;
- Comorbid conditions limiting probable life span to <4 years (e.g. cancer, AIDS) or indication of end-stage complications of diabetes (kidney dialysis, or transplant, blindness, or lower extremity amputation);
- Receiving treatment for a major psychiatric disorder (i.e. schizophrenia);
- Unable to give informed consent;
- Under the age of 18;
- Has no access to a telephone (Phone contact is a critical component of the intervention).
- Cannot walk 2 blocks without stopping and resting.
- Impaired cognitive function as determined by mini-mental test.
- Lives in the same household as an active LIFE participant.
- Presence of sickle cell trait
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Vårdstandard
|
Participants receive 2 diabetes education classes taught by a Certified Diabetes Educator.
They also receive diabetes education newsletters every 2 months.
|
|
Experimentell: Intensive education and support
|
Group classes for 12 months (weekly for 4 months, biweekly for 4 months, monthly for 4 months), weekly peer supporter telephone calls, and diabetes education newsletters every 2 months.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Hemoglobin A1c
Tidsram: change from baseline to 12 months
|
Finger prick on Afinion machine
|
change from baseline to 12 months
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Physical Activity
Tidsram: change from baseline to 12 months
|
An accelerometer is worn by participants for seven days.
International-Physical Activity Questionnaire is administered at baseline, 6 months, 1 year, and 18 months.
|
change from baseline to 12 months
|
|
Total Energy Intake
Tidsram: change from baseline to 12 months
|
24-hour dietary food recalls
|
change from baseline to 12 months
|
|
Physical Measures
Tidsram: change from baseline to 12 months
|
Measurements of weight, waist circumference, and blood pressure.
|
change from baseline to 12 months
|
|
Medications
Tidsram: change from baseline to 12 months
|
Participants bring all medications to the clinic visit and medication and dosage is recorded.
|
change from baseline to 12 months
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Elizabeth Lynch, PhD, Rush University Medical Center
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- Lynch EB, Mack L, Avery E, Wang Y, Dawar R, Richardson D, Keim K, Ventrelle J, Appelhans BM, Tahsin B, Fogelfeld L. Randomized Trial of a Lifestyle Intervention for Urban Low-Income African Americans with Type 2 Diabetes. J Gen Intern Med. 2019 Jul;34(7):1174-1183. doi: 10.1007/s11606-019-04894-y. Epub 2019 Apr 8.
- Lynch EB, Liebman R, Ventrelle J, Keim K, Appelhans BM, Avery EF, Tahsin B, Li H, Shapera M, Fogelfeld L. Design of the Lifestyle Improvement through Food and Exercise (LIFE) study: a randomized controlled trial of self-management of type 2 diabetes among African American patients from safety net health centers. Contemp Clin Trials. 2014 Nov;39(2):246-55. doi: 10.1016/j.cct.2014.09.003. Epub 2014 Sep 22.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 mars 2012
Primärt slutförande (Faktisk)
25 november 2015
Avslutad studie (Faktisk)
2 december 2015
Studieregistreringsdatum
Först inskickad
12 juli 2013
Först inskickad som uppfyllde QC-kriterierna
15 juli 2013
Första postat (Uppskatta)
17 juli 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
10 maj 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
8 maj 2017
Senast verifierad
1 maj 2017
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- 1R01DK092271-01 (U.S.S. NIH-anslag/kontrakt)
- R01DK092271-01 (U.S.S. NIH-anslag/kontrakt)
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