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Completed

NCT Number: NCT06739694

Neuroscience Education in Shoulder Pain: Clinical Trial

Objectives: The purpose of this study was to assess the efficacy of a pain neuroscience education programme applied to patients with shoulder pain.

Completed

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Eva

León, Spain, 24196

About this study

A randomised controlled trial was performed. Fifty-five patients satisfied eligibility criteria, agreed to participate, and were randomized into an experimental group (n = 27) or control group (n =28). A manual therapy and exercises program was administered for both groups. In addition, a pain neuroscience education protocol was administered for the experimental group for a whole period of 4 weeks (1 session/week, 75mins per session).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being 18-70 years of age.
  • History of shoulder pain of more than 3 months duration.
  • Presence of a painful arc
  • Medical diagnosis of shoulder pain with at least 2 positive impingement tests including Neer, Hawkins, or Jobe test

Exclusion criteria

  • Diagnosis of fibromyalgia.
  • Pregnancy.
  • A history of traumatic onset of shoulder pain.
  • Other histories of shoulder injury.
  • Torn tendons.
  • Ligamentous laxity based on a positive Sulcus and apprehension tests.
  • Numbness or tingling in the upper extremity.
  • Previous shoulder or cervical spine surgery.
  • Systemic illness.
  • Corticosteroid injection on the shoulder within 1 year of the study.
  • Physical therapy 6 months before the study.

Treatment and study plan

PNE

Behavioral

A manual therapy(Mulligan´s Mobilization with Movement) and 4 sessions of strenght exercises program was administered for both groups. In addition, a pain neuroscience education protocol was administered for the experimental group for a whole period of 4 weeks (1 session/week, 75mins per session).

Other names: Manual therapy, Exercise

Manual Therapy

Procedure

5 sessions of Mulligan´s Mobilization with Movement and 4 sessions of strenght exercises

Primary outcomes

  1. Pain

    Time frame: Baseline and 5 weeks.

    Reduction in pain intensity using the Shoulder Pain and Disability Index (SPADI)

  2. Disability

    Time frame: Baseline and five weeks.

    Improving functionality using the Shoulder Pain and Disability Index (SPADI)

Secondary outcomes

  1. kinesiophobia

    Time frame: Baseline and 5 weeks.

    Tampa Scale of Kinesiophobia (TSK11)

Other outcomes

  1. catastrophizing

    Time frame: Baseline and 5 weeks.

    Pain catastrophizing scale (PCS)

Sponsors and collaborators

Lead sponsor

Universidad de León

Other

Registry information

Official study title

The Efficacy of a Pain Neuroscience Education Programme in Shoulder Pain: a Randomised Clinical Trial

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Dec 18, 2024
Registry last updated
Dec 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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