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Rehabilitation after THA using a tailored web application: A pilot study

Completed
Conditions
hip wear
10023213
hip osteoarthritis
Registration Number
NL-OMON48132
Lead Sponsor
Reinier de Graaf Groep
Brief Summary

Trial is onging in other countries

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Planned THA within three to eight weeks
Age *18
Signed informed consent
Regular use of internet and e-mail.

Exclusion Criteria

Insufficient knowledge of the Dutch language
Mental disability

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Endpoints: Use and evaluation of the application by patients and care<br /><br>providers. After each consultation, patients will be interviewed about their<br /><br>experiences with the prototype. Participating care providers will also be<br /><br>interviewed at least once about their general experience with the prototype<br /><br>during consultations. In addition, web metrics will be recorded for each<br /><br>patient to assess usage over time. Parameter: The patient subgroups are used as<br /><br>parameter. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>As a secondary endpoint, experiences of participating patients will be<br /><br>qualitatively compared to those of a control sample (data from earlier<br /><br>qualitative studies.)</p><br>
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