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Home Rehabilitation After Hip Fracture

[Rehabilitación Domiciliaria Tras Fractura de Cadera] Home Rehabilitation After Hip Fracture

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07478445
Acronym
RECADO
Enrollment
80
Registered
2026-03-17
Start date
2024-02-01
Completion date
2025-09-30
Last updated
2026-03-19

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

Conditions

Hip Fractures (ICD-10 72.01-72.2), Home Care, Hospital-Based, Home Care Services

Keywords

Hospital at home, Multidisciplinary care, Patient Discharge, Physical Therapy Modalities, Functional Status, Adult, Aged, Hip Fractures, Home care services

Brief summary

This study will examine whether a home-based rehabilitation program can help older adults recover after surgery for a hip fracture. The program is delivered by a specialized "Hospital-at-Home" unit, which provides hospital-level care in the patient's home. Participants in this study are adults aged 65 years and older who have undergone hip fracture surgery at Hospital Universitari i Politècnic La Fe in Valencia, Spain. Instead of remaining in the hospital after surgery, participants will be admitted to the Hospital-at-Home program. A multidisciplinary medical team will provide comprehensive care at home, including medication management, wound care, and in-home physical therapy. The primary goal of the study is to assess recovery of walking ability and mobility within the home. The study will also evaluate overall functional improvement, frailty, and survival. Participants will be assessed at the start of the program and again at 45 days and 180 days after surgery. The information collected will help determine whether this type of home-based care is an effective option for supporting recovery and independence in older adults after a hip fracture. Recruitment for the study began in February 2024 and is expected to continue for one year.

Interventions

None listed

Sponsors

Instituto de Investigacion Sanitaria La Fe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* \- Patients aged 65 years or older undergoing surgery for traumatic hip fracture. * Ability to actively collaborate in the physiotherapy program. * Compliance with the UHD admission criteria (contact telephone number, identified caregiver, and residence within the geographical area of the Hospital Universitari i Politècnic La Fe).

Exclusion criteria

* \- Patients residing outside the geographical area covered by the La Fe hospital UHD. * Refusal to participate in the follow-up. * Clinical instability or end-of-life situation (oncologic or non-oncologic). * Cognitive impairment that prevents collaboration. * Institutionalized patients.

Design outcomes

Primary

MeasureTime frameDescription
Walking ability and home transfersassessed at different time points (prior, admission to the UHD, and at 45 and 180 days).Walking ability and home transfers, taken from the Barthel Index

Secondary

MeasureTime frameDescription
Functional improvementprior, admission to the UHD, and at 45 and 180 daysmeasured by the change of the Barthel Index
Mortality360 daysNumber of deaths
Frailty was assessed with the Rockwood Index at the time of admission, at baselineBaselineThe modified Clinical Frailty Scale (CFS) is a simple, 34-point clinical tool used by healthcare providers to quickly summarize a patient's overall level of fitness or frailty based on their mobility, energy, and function. It helps predict outcomes and guide care decisions in older adults.
Number of participants with all-cause readmission, delirium, wound infection, or bleeding15 daysSafety was assessed by monitoring the occurrence of all-cause readmissions, episodes of delirium, wound infection, or bleeding during the intervention period.
Change in quality of life assessed by the EuroQoL-5D questionnaireOne yearQuality of life was assessed using the EuroQol-5D-3L (EQ-5D-3L), a standardized instrument measuring health-related quality of life across five dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression), each with three levels. The descriptive system defines health states and does not itself yield a single score with fixed minimum and maximum values. Health states can be converted into a utility index typically ranging from values below 0 (worse than death) to 1 (full health), where higher scores indicate better health. Changes in quality of life will be assessed at 12 months

Countries

Spain

Contacts

PRINCIPAL_INVESTIGATORAna Torrego, MD, PhD

Hospital at Home Unit - Hospital UiP La Fe Valencia Avda Fernando Abril Martorell 106 Torre B Planta 1 Valencia 26206 (SPAIN)

STUDY_CHAIRAna Soler, MD, PhD

Physical Medicine and Rehabilitation Service (SMFR); Hospital UiP La Fe Valencia Avda Fernando Abril Martorell 106

STUDY_CHAIRElisa Soriano, MD, PhD

Hospital at Home Unit Hospital UiP La Fe Valencia Avda Fernando Abril Martorell 106 Torre B Planta 1 Valencia 26206 (SPAIN)

PRINCIPAL_INVESTIGATORMarta Muñoz Domingo, Senior Technician / Research C

Universitat Politècnica de València (UPV) Centro de Investigación de Ingeniería Económica (CIEGS)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026