Self-Management for Persistent Subacromial Pain

NCT04190836 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2019-12-09

No results posted yet for this study

Summary

Physiotherapy-led exercises is the first line treatment for patients with subacromial pain. However, current evidence report that most treatment programmes only show a short-term benefit. There seem to be a potential for enhancing the effectiveness of exercise interventions by improving adherence to self-managed exercises, but there is lack of knowledge about adherence to exercise programmes in shoulder pain. Before conducting a planned randomised controlled trial on the clinical effectiveness of an intervention focusing on adherence to a self-managed exercise strategy (the Ad-Shoulder intervention), it is necessary to run a feasibility study in order to establish whether such a resource-demanding trial is worthwhile. Feasibility studies are designed to answer the key question "Can it work?" The main objectives of the present study was to assess the feasibility in terms of recruitment capability, data collection procedures and acceptability of the Ad-Shoulder intervention in patients with subacromial pain receiving treatment in primary or secondary health care.

Conditions

  • Shoulder Pain Chronic

Interventions

BEHAVIORAL

Self-Managed Exercise Strategy

The intervention is a personalised supported self-management intervention which emphasises dynamic, progressively loaded exercises for the shoulder. The intervention consisted of 1-5 individual sessions provided over 3 months, with a duration of 1 hour for the first session and 45 minutes for the following. The participants will have the opportunity to contact the physiotherapist by phone, text message or e-mail for advice during the treatment period (12 weeks). The personalised supported self-management intervention will be based on the components of the self-management framework, provided by Lorig and Holman (2003). The five self-management skills and the operationalization of these will be described when publishing the study. For specific content reporting of the self managed exercises we will follow the Consensus on Exercise Reporting Template.

Sponsors & Collaborators

  • Oslo University Hospital

    collaborator OTHER
  • Keele University

    collaborator OTHER
  • National Institute of Occupational Health

    collaborator UNKNOWN
  • Diakonhjemmet Hospital

    collaborator OTHER
  • Oslo Metropolitan University

    lead OTHER

Principal Investigators

  • Daniel Major, MSc · Oslo Metropolitan University

  • Yngve Røe, PhD · Oslo Metropolitan University

  • Margreth Grotle, PhD · Oslo Metropolitan University

  • Chris Littlewood, PhD · Keele University

  • Dagfinn Matre, PhD · National Institute of Occupational Health, Norway

  • Heidi V Gallet, MSc · Diakonhjemmet Hospital

  • Hege Bentzen, PhD · Oslo Metropolitan University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2018-09-12
Completion
2018-09-12

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04190836 on ClinicalTrials.gov