Digitally Assisted Rehabilitation at Home for Older Adults After Hip Surgery (GRIMSEL)
GRIMSEL
Digitally Assisted Geriatric Home-rehabilitation in Older Patients After Hip Surgery (GRIMSEL): a Non-inferiority Randomized Controlled Trial
1 other identifier
interventional
66
0 countries
N/A
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2026
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 8, 2026
CompletedFirst Posted
Study publicly available on registry
June 22, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2028
June 22, 2026
June 1, 2026
1.1 years
June 8, 2026
June 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
FIM motor subscale
Change of the Functional independence measure (FIM) motor subscale from baseline to follow-up (12 weeks after surgery) between intervention and control group. The FIM motor subscale is a 13-item assessment tool ranging from a minimum of 13 points (dependence) to a maximum of 91 points (independence)
from baseline (day 1 post-surgery) to follow-up (12 weeks after surgery)
Study Arms (2)
Routine care
ACTIVE COMPARATORRoutine care (outpatient physiotherapy)
Digitally supported multimodal home rehabilitation
EXPERIMENTALInterventions
Multimodal personalized rehabilitation program including the medical application Akina and self-managed care based on a geriatric assessment
Eligibility Criteria
You may qualify if:
- Community-dwelling adults aged 55 to 80 years
- Hospitalized for hip surgery with unrestricted weight bearing at University Hospital Bern
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 8, 2026
First Posted
June 22, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
September 1, 2027
Study Completion (Estimated)
August 1, 2028
Last Updated
June 22, 2026
Record last verified: 2026-06