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    <responseDate>2026-10-15T08:49:39Z</responseDate>
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            <header>
                <identifier>oai:data.mendeley.com/h4bmjrs7gc.2</identifier>
                <datestamp>2020-07-15T13:10:45Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Brekke, Anders Falk</dc:creator>
    <dc:title>Exercise in patients with acetabular retroversion and excessive anterior pelvic tilt: A feasibility and intervention study</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Objectives: To investigate feasibility and change in patient-reported symptoms of a home-based exercise intervention in patients with acetabular retroversion and excessive anterior pelvic tilt, in comparison with a prior control period.

Design: Following baseline examinations, an 8-week control period was followed by an 8-week home-based exercise period. Subsequently, the patients were encouraged to continue with the exercise program for additional 16 weeks. 

Outcomes: Good feasibility was defined as; a ´dropout´ rate ≤10%, ´adherence´ to the exercise program as ≥75% completion (18 out of 24 sessions), the ratio of training sessions increasing pre to post ´exercise-related pain´ (NRS &gt;4) should not increase, no serious ´exercise-related adverse events´, and usage of ´hip-related analgesics´ should not increase. Parameters regarding feasibility and general comments on the exercise program were recorded in the self-reporting training diary.
Primary endpoint was HAGOS-PAIN subscale after the 8-week exercise period. Secondary endpoints were the remaining five HAGOS-subscales, EQ-5D-3L, and change in pelvic tilt (sagittal inclination in degrees) measured with low-dose radiation EOS® scanning in standardized standing position.

One data set contains raw anonymous data for the complete exercise intervention at four time-points: T1) baseline, T2) start-up of exercise intervention 8 weeks from baseline, T3 end of exercise intervention after 8 weeks (primary endpoint), and T4 follow-up after 16-weeks. The second data set contains data from the training diaries. 

ClinicalTrials.gov: NCT03578562
</dc:description>
    <dc:subject>Clinical Intervention</dc:subject>
    <dc:subject>Feasibility Study</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/h4bmjrs7gc.2</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/h4bmjrs7gc.2</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:relation>https://data.mendeley.com/datasets/h4bmjrs7gc</dc:relation>
    <dc:date>2020-07-15T13:10:45Z</dc:date>
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