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Motivational Interventions and Physical Exercise in Patients With Fragility Fracture

Effectiveness of a Follow-up Program Based on Motivational Interventions and Physical Exercise in Patients With Fragility Fracture: Randomized Controlled Clinical Trial.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04934358
Acronym
PREVFRAILTY
Enrollment
100
Registered
2021-06-22
Start date
2022-01-10
Completion date
2024-12-31
Last updated
2024-04-03

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

Conditions

Fragility Fracture

Keywords

fragility fracture, physical exercise, motivational intervention

Brief summary

Patients with a fragility fracture are twice as likely to have future fractures compared to their non-fractured peers. Furthermore, the 30% who suffer a fragility fracture do not regain the level of functioning in terms of activities of daily living after one year. A recent ecological study, in several European countries, estimates that if fracture patients were enrolled in fracture follow-up services, at least 19,000 fractures could be prevented each year. Clinical trials carried out in the research group have shown that the prescription of physical exercise in severe underlying pathologies is effective in improving physical function, quality of life and long-term results. Hypothesis: The implementation of a motivational intervention and physical exercise program, in a staggered manner, taking into account the basic exercise capacity, improves the functional status of the patient (basic activities of daily life), adherence to interventions and the level of physical activity, and therefore reduces the number of hospital admissions, refractures and other associated complications. Objective: To evaluate the effect of a rehabilitation intervention based on physical exercise and motivation, applied in a staggered manner and according to the functional capacity of patients with fragility fracture.

Detailed description

Method: Single-blind, randomized, controlled clinical study, with 2 parallel arms and single-center. Study subjects: Patients who underwent surgery for a fragility hip fracture between September 2021 and September 2022 in a tertiary hospital in southern Spain. A progressive physical exercise and motivational intervention adjusted for functional capacity will be compared versus usual rehabilitation care. Follow-up of patients for 3 months and a final visit at 6 months. The primary outcome variables will be functional status for the development of activities of daily living (individual ability to care for himself) and number of hospital readmissions (reasons and consequences). Variables related to quality of life, cognitive status, laboratory markers and densitometry will also be analyzed.

Interventions

BEHAVIORALPhysical and motivational follow-up treatment

Physical and motivational follow-up treatment

BEHAVIORALUsual care

Usual rehabilitation program

Sponsors

Maimónides Biomedical Research Institute of Córdoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

Single (Investigator)

Intervention model description

Parallel Assignment

Eligibility

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

Inclusion criteria

* Present a hip fracture (includes cervical fracture and trochanteric), classified in the 10th version of the International Classification of Diseases (ICD-10-ES) with codes S72-S72.26X; * In addition, the fracture must be due to fragility: fracture due to a low-energy trauma or not proportional to the consequences (Hermoso de Mendoza, 2003); * To have received a surgical repair by replacement arthroplasty or internal fixation (ICD-10-ES procedures: 0SU and 0SR) in a period of less than one week; * To be recovering in a trauma and orthopedic unit and/or be transferred to a rehabilitation unit or discharged; * Before the fracture, independent or mild dependence for activities of daily living (Barthel index\> 60) and living at home; * To have the cognitive ability to give informed consent (ANNEX I); * To live and be domiciled in a basic health area covered by the study hospital complex * To be over 50 years of age

Exclusion criteria

* Presence of low cognitive level (scores below 23 points in Lobo's Mini-cognitive exam); * Patients with pathological fractures due to skeletal alterations other than osteoporosis; * Presence of more than one fall (other than the cause of hospital admission) in the last year; * Presence of uncorrected anemia (hemoglobin concentration \<9/dL), acute infectious disease (C-reactive protein\> 10 mg / L), severe cardiorespiratory disease (for example: unstable angina; severe heart failure identified by the New York Heart Association as class III-IV), musculoskeletal or neurological diseases (for example, major amputation of lower limbs) that make physical exercise impossible.

Design outcomes

Primary

MeasureTime frameDescription
Barthel index6 monthsFunctional status for the development of activities of daily living (individual ability to take care of himself)
Number of hospital readmissions6 monthsOther clinical outcomes, such as mortality and all-cause hospitalization,

Secondary

MeasureTime frameDescription
Geriatric Depression Scale6 monthsis a brief, 30-item questionnaire in which participants are asked to respond by answering yes or no in reference to how they felt over the past week
Visual analogue scale6 monthsA validated, subjective measure for acute and chronic pain
Mini-Mental State Examination6 monthsA 30-point questionnaire that is used extensively in clinical and research settings to measure cognitive impairment
5-level EQ-5D version6 monthsA standardised measure of health-related quality of life
Falls Efficacy Scale-International6 monthsIt is a 16 item questionnaire, useful to the researchers and clinicians interested in fear of falling, with a score ranging from minimum 16 (no concern about falling) to maximum 64 (severe concern about falling)
Minnesota Leisure Time Physical Activity Questionnaire6 monthsTo assess the quantity (total activity metabolic index) and quality (heavy, moderate, and light) of physical activity performed

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 31, 2026