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Not yet recruiting NCT07658664

Digitally Assisted Rehabilitation at Home for Older Adults After Hip Surgery (GRIMSEL)

No phase Interventional Hip Surgery Rehabilitation Program Geriatrics Rehabilitation Digital Health Intervention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Digitally supported multimodal rehabilitation program, routine care.
Who it may be relevant to
Registry conditions: Hip Surgery, Rehabilitation Program, Geriatrics Rehabilitation, Digital Health Intervention. Basic parameters: 55 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Digitally Assisted Geriatric Home-rehabilitation in Older Patients After Hip Surgery (GRIMSEL): a Non-inferiority Randomized Controlled Trial

Overview

The goal of this clinical trial is to learn if a 12-week digitally supported, multimodal home rehabilitation program using the medical application Akina is as effective compared to routine care regarding functional independence in older adults undergoing hip surgery. How is this multimodal home rehabilitation program received by patients? Is this multimodal home program at least as effective in terms of functional indpendence, muscle status, mobility and quality of life compared to routine care? Researchers will compare the multimodal rehabilitation program using the application Akina to routine care to see if the program works to treat patients after hip surgery. Participants will: Undergo the rehab program at home or receive routine care (outpatient physiotherapy) for 12 weeks Visit the clinic after 6 and 12 weeks

Interventions

  • Other Digitally supported multimodal rehabilitation program
    Multimodal personalized rehabilitation program including the medical application Akina and self-managed care based on a geriatric assessment
  • Other routine care
    routine care

Primary outcome measures

  • FIM motor subscale [Time frame: from baseline (day 1 post-surgery) to follow-up (12 weeks after surgery)]

Eligibility criteria

Inclusion criteria

  • Community-dwelling adults aged 55 to 80 years
  • Hospitalized for hip surgery with unrestricted weight bearing at University Hospital Bern

Exclusion criteria

  • Discharge to inpatient rehabilitation
  • inability to comply with a rehabilitation program (e.g. comorbidity that prevents 30min light workout, major cognitive impairment)
  • end-of life situation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07658664 · BASEC 2026-D0032

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗