Proprioception and BRACE Training in Knee Osteoarthritis

NCT ID: NCT04782167

Last Updated: 2023-08-14

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-06-01

Study Completion Date

2020-11-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Knee osteoarthritis is common joint disorder in older adults. The prevalence of osteoarthritis is increasing in the elderly population and due to obesity.The aim of this study to compare improvement in balance between BRACE and proprioceptive training in knee osteoarthritis and to compare mobility level between proprioceptive and BRACE in knee osteoarthritis

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Knee osteoarthritis is common joint disorder in older adults. The prevalence of osteoarthritis is increasing in the elderly population and due to obesity. Balance disorder generally disturbed equilibrium and increase risk of fall. There is lack of proprioceptive sensation in patients with knee osteoarthritis. The aim of this study to compare improvement in balance between BRACE and proprioceptive training in knee osteoarthritis and to compare mobility level between proprioceptive and BRACE in knee osteoarthritis. Randomized control trial study of 8 week follows up. Sample size will be 22. The patients will be divided into 2 groups BRACE and proprioceptive training. The patients will get training section for 3 days per week for 8 weeks. The measurement will be taken at base line, after 8 weeks. Study duration will be 6 months. Individuals of age 50-70 year, Mini-mental state examination (MMSE) 20 or higher, Berg Balance Scale (BBS) 30-45 points, Experience of at least one fall during the previous 12 months, both Males and Females will be include. Patients will be excluded if they exhibited history of cardiovascular or musculoskeletal diseases, previously used medication for the central nervous system, occurrence of lower limbs lesions or fractures in last six months. Assessment tools will be MMSE, Berg balance scale, TUG, CTSIB, 6 minute walk test. Data will be analyzed through SPSS 20. Data will be check for its normality, within groups comparison paired sample T-test, between groups independent sample T-test will be used

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteoarthritis Knees Both

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Proprioception training

Researcher give proprioception protocol to one group

Group Type EXPERIMENTAL

Propirioceptive training

Intervention Type BEHAVIORAL

1st Phase - Steady phase (1st set: Eyes Open, 2nd set: Eyes Close) Preserve standup position Equally heels up and down Preserve standup on one leg by turns

Brace

Researcher give BRace training to one group

Group Type EXPERIMENTAL

BRACE

Intervention Type BEHAVIORAL

Balance training,Static balance:

1. Romberg with eye open \& eye close \[30 sec repeat 3 times\]
2. Tandem standing with eye open then with eye close. Right foot front first, then left foot front \[10 Sec repeat 3 times\]
3. Single leg stance 5 repetition with sec.

Static/Dynamic/Anti-cipatory Postural Control:

1. Sit to stand: 5 repetition
2. Functional reach test: forward, sideways \& cross reach, practice 1 min for each
3. TUG test: with distance of 10 feet \& time 10 sec. practice 2 min Cognitive exercises

1\) Count reverse from 50 Repeat with eyes open and close Reps of 30s for each 2) Push wall and reverse count from 20 3) Remember 5 words, Name 5 animals, Repeat 5 words

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

BRACE

Balance training,Static balance:

1. Romberg with eye open \& eye close \[30 sec repeat 3 times\]
2. Tandem standing with eye open then with eye close. Right foot front first, then left foot front \[10 Sec repeat 3 times\]
3. Single leg stance 5 repetition with sec.

Static/Dynamic/Anti-cipatory Postural Control:

1. Sit to stand: 5 repetition
2. Functional reach test: forward, sideways \& cross reach, practice 1 min for each
3. TUG test: with distance of 10 feet \& time 10 sec. practice 2 min Cognitive exercises

1\) Count reverse from 50 Repeat with eyes open and close Reps of 30s for each 2) Push wall and reverse count from 20 3) Remember 5 words, Name 5 animals, Repeat 5 words

Intervention Type BEHAVIORAL

Propirioceptive training

1st Phase - Steady phase (1st set: Eyes Open, 2nd set: Eyes Close) Preserve standup position Equally heels up and down Preserve standup on one leg by turns

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 50-70 years.
* Both Males and Females
* Knee osteoarthritis unilateral and bilateral (12).
* American College of Rheumatology (ACR) criteria for diagnosing osteoarthritis of knee joint is presence of pain in knee joint plus any three of six factors listed below (13).
* Age more than 50 y
* Presence of crepitus on active motion
* Less than 30 min of morning stiffness
* Bony tenderness
* Bony overgrowth
* No palpable warmth of synovium
* Mini-mental state examination (MMSE) 23 or higher (14).
* Berg Balance Scale (BBS) 30-45 points (4)

Exclusion Criteria

* History of stroke during the previous 12 months
* History of cardiovascular or musculoskeletal diseases,

* Previously used medication for the central nervous system.
* Presence of lower limb lesions or fractures in the last six months
Minimum Eligible Age

50 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

khadija liaquat

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

khadija liaquat

Senior Lecturer

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Independent University Hospital, faisalabad

Faisalābad, Punjab Province, Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Riphah IU Ali

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.