Skip to content

Multi-Modal Intervention In Frail And Prefrail Older People With Type 2 Diabetes

A RANDOMIZED CLINICAL TRIAL TO EVALUATE THE EFFECTIVENESS OF A MULTI-MODAL INTERVENTION IN FRAIL AND PREFRAIL OLDER PEOPLE WITH TYPE 2 DIABETES ON FRAILTY AND QUALITY OF LIFE: THE MID-Frail STUDY

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01654341
Acronym
MID-Frail
Enrollment
986
Registered
2012-07-31
Start date
2013-12-31
Completion date
2017-02-28
Last updated
2019-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes Mellitus

Brief 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.

Detailed 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.

Interventions

BEHAVIORALExercise, dietary and educational program

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Changes in summary ordinal score on the Short Physical Performance Battery test2 yearsThe 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.

Secondary

MeasureTime frameDescription
Barthel index of activities of daily living2 years
Euro-Quality of Life (QoL) index2 years
Economic costs/healthcare expenditure due to diabetes and its impact on disability and quality of life,2 yearsEconomic 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).
Symptomatic hypoglycaemia2 yearsEpisodes 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)
Lawton Instrumental Activity of Daily Living (IADL) scale2 years
Episodes of permanent institutionalization2 yearsEpisodes 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).
Caregiver Strain Index2 yearsBurden of the carer, as assessed by the modified Caregiver Strain Index
Mortality2 years
Hospital admissions2 yearsEpisodes of hospital admission (i.e., any admission involving an overnight stay)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026