An interventional study of Digitally supported multimodal rehabilitation program and routine care in Hip Surgery, Rehabilitation Program and Geriatrics Rehabilitation, sponsored by Insel Gruppe AG, University Hospital Bern. Not yet recruiting. Open to participants aged 55 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-06-22.
Sponsored by Insel Gruppe AG, University Hospital Bern · Not applicable, Interventional, and Health services research
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
Insel Gruppe AG, University Hospital Bern is the lead sponsor of 724 studies on the registry; 177 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Routine care (outpatient physiotherapy)
Other: routine care
Other: Digitally supported multimodal rehabilitation program
Multimodal personalized rehabilitation program including the medical application Akina and self-managed care based on a geriatric assessment
routine care
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)
Time frame: from baseline (day 1 post-surgery) to follow-up (12 weeks after surgery)
No study locations are listed for this record.
This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.
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Insel Gruppe AG, University Hospital Bern