Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01654341
Other study ID # MID-Frail
Secondary ID 278803-2
Status Completed
Phase N/A
First received
Last updated
Start date December 2013
Est. completion date February 2017

Study information

Verified date March 2019
Source Hospital Universitario Getafe
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The MID-Frail STUDY project focuses on the use of interventions designed to improve functional status and enhance quality of life (rather than traditional treatments such as glucose- and blood pressure- lowering) by acting on the mechanisms involved in producing frailty and its progression to adverse outcomes.


Description:

Detailed Description: Subjects enrolled in the main study will also be invited to join the following sub-studies:

GENEFRAIL: this sub-study aims to determine the polymorphisms of several genes associated to frailty, in order to establish its predictive value for developing disability and response to treatment as well METABOFRAIL: this sub-study aims to investigate the metabolomic profile of frail and pre-frail patients. SARTRAIN: the combination of the assessment tools used in SARTRAIN (ARFI US, MRI, posturographic measurements) will provide a comprehensive study of the structural and functional characteristics of muscle and adjacent tissues and their change with time and the intervention. MID- POW: this sub-study aims to investigate changes in muscle power.

The project also include an randomized controlled ancillary study: SENSOLE for which the aim is to investigate the potential effects of vibrating insoles device on gait and posture.


Other known NCT identifiers
  • NCT01541787

Recruitment information / eligibility

Status Completed
Enrollment 986
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion criteria:

- Participant is willing and able to give written informed consent for participation in the study.

- Subjects aged 70 years or older, with a diagnosis of type 2 diabetes mellitus for at least 2 years.

- Require to fulfill Fried ´s criteria for frail or pre-frail individuals.

Exclusion criteria:

- Barthel score lower than 60 points.

- Inability to carry out SPPB test (total score=0).

- Mini Mental State Examination score less than 20 points.

- Subjects unwilling or unable to consent or unable to participate safely in intervention program.

- Previous history of myocardial infarction within 6 months, unstable angina or congestive heart failure in III-IV NYHA stage.

- Clinically instable patients in the clinical judgment of the investigator.

- Terminal illness (life expectancy < 6 months).

- Any other condition that, in the clinical judgment of the investigator, means that it would not in the patient's best interests to enter the study.

- Current participation in clinical trial or any other investigational study.

Study Design


Intervention

Behavioral:
Exercise, dietary and educational program


Locations

Country Name City State
Spain Hospital Universitario de Getafe Madrid Getafe

Sponsors (15)

Lead Sponsor Collaborator
Hospital Universitario Getafe Cardiff University, Catholic University of the Sacred Heart, Diabetes Frail Ltd, Hexabio Sarl, Igen Biotech SL, Niche Science & Technology Ltd, University Ghent, University Hospital, Bordeaux, University Hospital, Toulouse, University of Campania "Luigi Vanvitelli", University of Castilla-La Mancha, University of Ulm, Univerzita Karlova v Praze, Vrije Universiteit Brussel

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in summary ordinal score on the Short Physical Performance Battery test The Short Physical Performance Battery (SPPB) is a simple test to measure lower extremity function using tasks that mimic daily activities. The SPPB examines 3 areas of lower extremity function; static balance, gait speed, and getting in and out of a chair. These areas represent essential tasks important for independent living and are thus an important outcome measure for patients with cardiovascular and pulmonary disease. 2 years
Secondary Lawton Instrumental Activity of Daily Living (IADL) scale 2 years
Secondary Barthel index of activities of daily living 2 years
Secondary Euro-Quality of Life (QoL) index 2 years
Secondary Economic costs/healthcare expenditure due to diabetes and its impact on disability and quality of life, Economic costs/healthcare expenditure due to diabetes and its impact on disability and quality of life, using an economic model embracing the direct health-related costs (in-patient, out-patient, pharmaceutical, etc), formal care costs (home care, respite care, day centers, etc) and the informal care costs (carer). 2 years
Secondary Symptomatic hypoglycaemia Episodes of symptomatic hypoglycaemia (i.e., a recorded blood sugar less than 4 mmol/L, or symptoms or signs attributed to low blood sugar and responding to appropriate treatment) 2 years
Secondary Hospital admissions Episodes of hospital admission (i.e., any admission involving an overnight stay) 2 years
Secondary Episodes of permanent institutionalization Episodes of permanent institutionalization (i.e., permanent move to any care setting other than the patient's own home, where paid staff are available to provide care if needed at any time during the day or night). 2 years
Secondary Caregiver Strain Index Burden of the carer, as assessed by the modified Caregiver Strain Index 2 years
Secondary Mortality 2 years
See also
  Status Clinical Trial Phase
Completed NCT02771093 - An Exploratory Study of the Effects of Trelagliptin and Alogliptin on Glucose Variability in Patients With Type 2 Diabetes Mellitus Phase 4
Completed NCT02545842 - Assessment Study of Three Different Fasting Plasma Glucose Targets in Chinese Patients With Type 2 Diabetes Mellitus (BEYOND III/FPG GOAL) Phase 4
Recruiting NCT03436212 - Real-Life Home Glucose Monitoring Over 14 Days in T2D Patients With Intensified Therapy Using Insulin Pump. N/A
Completed NCT03244800 - A Study to Investigate Different Doses of 0382 in Overweight and Obese Subjects With Type 2 Diabetes Mellitus. Phase 2
Completed NCT03960424 - Diabetes Management Program for Hispanic/Latino N/A
Withdrawn NCT02769091 - A Study in Adult Patients With Nonalcoholic Steatohepatitis Who Also Have Type 2 Diabetes Phase 2
Recruiting NCT06065540 - A Research Study to See How Well CagriSema Compared to Semaglutide, Cagrilintide and Placebo Lowers Blood Sugar and Body Weight in People With Type 2 Diabetes Treated With Metformin With or Without an SGLT2 Inhibitor Phase 3
Recruiting NCT05008276 - Puberty, Diabetes, and the Kidneys, When Eustress Becomes Distress (PANTHER Study)
Completed NCT04091373 - A Study Investigating the Pharmacokinetics of a Single Dose Administration of Cotadutide Phase 1
Completed NCT03296800 - Study to Evaluate Effects of Probenecid, Rifampin and Verapamil on Bexagliflozin in Healthy Subjects Phase 1
Recruiting NCT06212778 - Relationship Between Nutritional Status, Hand Grip Strength, and Fatigue in Hospitalized Older Adults With Type 2 Diabetes Mellitus.
Completed NCT05979519 - Fresh Carts for Mom's to Improve Food Security and Glucose Management N/A
Recruiting NCT05579314 - XW014 in Healthy Subjects and Patients With Type 2 Diabetes Mellitus (T2DM) Phase 1
Completed NCT03859934 - Metabolic Effects of Melatonin Treatment Phase 1
Terminated NCT03684642 - Efficacy and Safety of Efpeglenatide Versus Dulaglutide in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin Phase 3
Completed NCT03248401 - Effect of Cilostazol on Carotid Atherosclerosis Estimated by 3D Ultrasound in Patients With Type 2 Diabetes Phase 4
Completed NCT03644134 - A Personalized Intervention to Manage Physiological Stress and Improve Sleep Patterns N/A
Completed NCT05295160 - Fasting-Associated Immune-metabolic Remission of Diabetes N/A
Completed NCT02836873 - Safety and Efficacy of Bexagliflozin in Type 2 Diabetes Mellitus Patients With Moderate Renal Impairment Phase 3
Completed NCT02252224 - Forxiga (Dapagliflozin) Regulatory Postmarketing Surveillance