Patients Experiences of Rehabilitation Before and After Reverse Shoulder Arthroplasty

NCT ID: NCT06897124

Last Updated: 2025-06-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

15 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-04-21

Study Completion Date

2022-10-23

Brief Summary

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Reverse shoulder arthroplasty is a complex surgical procedure requiring thorough rehabilitation, and its frequency is increasing globally. While previous studies have quantitatively examined postoperative outcomes, such as pain levels and shoulder function, no research has yet explored patients' subjective experiences of the rehabilitation process before and after surgery. Purpose of the study was to explore patients' experiences of undergoing reverse shoulder arthroplasty and the associated rehabilitation process.

Detailed Description

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Surgery with total shoulder arthroplasty is a procedure that has increased in number in the last twenty years, and it is the third most common prosthetic surgery in the world after hip and knee. There are two types of shoulder arthroplasty, anatomical and reverse. When the rotator cuff is severely impaired or completely dysfunctional, a reverse shoulder prosthesis is used, in which the anatomical positions of the ball and socket are reversed.

There are thus several factors that the treating physiotherapist needs to take into account. Research on reverse shoulder arthroplasty has primarily focused on evaluations using quantitative measures. Qualitative research from the patient's perspective can provide a deeper understanding of their expectations and experiences, offering insights that complement and fill the gaps left by quantitative research. Gaining insight into patients' experiences would be valuable for physiotherapists working with this group, as it may help identify areas for improvement in care to better meet patients' needs.

Conditions

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Osteoarthritis of the Shoulder

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Women and men, who had undergone surgery with reverse shoulder arthroplasty.

The participants were recruited from three different hospitals in Western Sweden: a local hospital, a county hospital, and a university hospital. The inclusion criteria encompassed patients who had undergone elective surgery involving reverse shoulder arthroplasty in the Västra Götaland region who demonstrated proficiency in both spoken and written Swedish.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

Inclusion Criteria:

The inclusion criteria encompassed patients who had undergone elective surgery involving reverse shoulder arthroplasty in the Västra Götaland region who demonstrated proficiency in both spoken and written Swedish.

Exclusion Criteria:

Exclusion criteria applied to cases where the study leader had served as the patient's physiotherapist, the presence of neurological disorders, or the occurrence of surgical complications, such as infection or fracture.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Vastra Gotaland Region

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anette Larsson, RPT, PhD

Role: STUDY_CHAIR

Research, Education, Development & Innovation, Primary Health Care, Region Västra Götaland, Sweden.

Locations

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Research, Education, Development & Innovation, Primary Health Care, Region Västra Götaland, Sweden

Alingsås, Västra Götaland County, Sweden

Site Status

Countries

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Sweden

Other Identifiers

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VGFOUSA-1020701

Identifier Type: -

Identifier Source: org_study_id

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