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NCT06041100

What Are the Effects of a Bilateral Hip Exoskeleton During Daily Use by 65+ Adults?

Completed NA Last updated 1 February 2024
What this trial tests

NA trial testing Exoskeleton in Pre-frail Senior Adults in 16 participants. Completed in 31 January 2024.

Timeline
6 September 2023
Primary endpoint
30 January 2024
31 January 2024

Quick facts

Lead sponsorAalborg University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment16
Start date6 September 2023
Primary completion30 January 2024
Estimated completion31 January 2024
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Aalborg University

Who can join

Adults 65 to 85, any sex, with Pre-frail Senior Adults. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Despite the huge popularity exoskeletons have gained in the past years and the benefits that they have shown to provide to users, there are still many aspects of wearing an exoskeleton that have yet to be determined. Therefore, the main objective of this study is to evaluate the feasibility using the acceptability of incorporating a passive assistive bilateral exoskeleton into the daily routine of pre-frail adults for a duration of 12-weeks. The second aim of the study is to determine whether this effect can be sustained even after a period of 6-weeks following the cessation of usage.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Exoskeleton

Trials testing the same drug.

Other Aalborg University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06041100.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing