Balance in People With Frozen Shoulder

Completed

• Conditions: Frozen Shoulder
• Interventions: Other: There was no intervention in this study.

• Registration Number: NCT06391567
• Lead Sponsor: Kirsehir Ahi Evran Universitesi

Brief Summary

The aim of this study was to investigate the balance characteristics of patients with Frozen Shoulder.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-10-10
• Status Verified: 2024-04
• Primary Completion: 2024-04-10
• Study Completion: 2024-04-16
• Study First Submitted: 2024-04-18
• Study First Submitted QC: 2024-04-25
• Last Update Submitted: 2024-04-25
• Study First Posted: 2024-04-30
• Last Update Posted: 2024-04-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

• Volunteers aged 40-65 years,
• Diagnosed with unilateral Frozen Shoulder, Frozen Shoulder stage 2-3,
• Pain lasting more than 3 months,
• No mental or cognitive impairment
• At least 25% movement limitation in at least 2 movement planes and
• Able to cooperate.

Exclusion Criteria

• Who had a neurological, rheumatic, cardiac and active malignant diseases
• Who had a history of surgery, trauma, and fracture
• Who had comorbid conditions that would affect balance

The control group consisted of healthy subjects who were not diagnosed with Frozen Shoulder and did not have a chronic disease that would affect balance between the ages of 40-65.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Control Group	There was no intervention in this study.	The control group consisted of healthy subjects who were not diagnosed with Frozen Shoulder and did not have a chronic disease that would affect balance between the ages of 40-65.
Patient Group	There was no intervention in this study.	Patients who were diagnosed with Frozen Shoulder by physical examination, met the inclusion criteria, and agreed to participate in the study were selected for the patient group.

Primary Outcome Measures

Name	Time	Method
Static and Dynamic Postural Balance	8 week	Biodex Balance System was used for objective assessment of static and dynamic postural balance. A high balance score indicates poor balance performance.
Pain Intensity	8 week	The pain intensity of the patients was measured using the Visual Analogue Scale. The pain intensity score ranges from 0 to 10. An increase in the score indicates an increase in pain; a decrease in the score indicates a decrease in pain.
Sociodemographic Form	8 week	Sociodemographic information of the patients included in the study, such as age, gender, height, weight, BMI, educational status, dominant side, comorbid status, and clinical information such as affected side, pain intensity, and pain duration were collected in a case report form by face-to-face interview
Balance Function	8 week	Balance function was measured with the Timed Up and Go Test (TUG). The TUG is a short, simple, and reliable test used to assess balance. It shows that people who complete the test in less than 20 seconds are independent in transfers, while people who complete the test in 30 seconds or more are more dependent in activities of daily living.

Trial Locations

Locations (1)

Atahan TURHAN; 🇹🇷 Kirsehir, Merkez, Turkey