NCT07658664

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
24mo left

Started Aug 2026

Typical duration for not_applicable

Status
not yet recruiting

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

Completed
14 days until next milestone

First Posted

Study publicly available on registry

June 22, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2028

Last Updated

June 22, 2026

Status Verified

June 1, 2026

Enrollment Period

1.1 years

First QC Date

June 8, 2026

Last Update Submit

June 16, 2026

Conditions

Keywords

functional independencehome-based rehabilitationself-managementorthogeriatrics

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 COMPARATOR

Routine care (outpatient physiotherapy)

Other: routine care

Digitally supported multimodal home rehabilitation

EXPERIMENTAL
Other: Digitally supported multimodal rehabilitation program

Interventions

Multimodal personalized rehabilitation program including the medical application Akina and self-managed care based on a geriatric assessment

Digitally supported multimodal home rehabilitation

routine care

Routine care

Eligibility Criteria

Age55 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Anna K. Eggimann, PD Dr. med.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Open-label, assessor-blinded, non-inferiority randomized clinical trial
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