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The Impact of Matrix Rhythm Therapy on Hand Movement and Function After hand Surgery.

The Effect of Matrix Rhythm Therapy (MaRhyThe®) on Hand Mobility and Function in Individuals with Post-Operative Hand Tendon Injuries: A Pilot Study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077550
Enrollment
10
Registered
2024-12-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M662- Spontaneous rupture of extensor tendons Health Condition 2: M663- Spontaneous rupture of flexor tendons

Interventions

Intervention1: Matrix Rhythm Therapy (MaRhyThe®): 6-months study application of Matrix Rhythm Therapy (MaRhyThe®) in Individuals with Post-Operative Hand Tendon Injuries Control Intervention1: Not App

Sponsors

Patil Aarti Bharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group: 18–60 years, with post-operative tendon injuries in the hand. 2. All genders are eligible to participate. 3. Referred cases of post-operative hand tendon injuries with a 6 to 8-week post-operative duration. 4. Participants with either flexor or extensor tendon injuries in the hand, at any zone, accompanied by hand mobility and function following a post-operative procedure. 5. Participants are willing to take part in the study and be able to understand instructions.

Exclusion criteria

Exclusion criteria: 1. history of tendon surgeries performed more than a year ago, especially those who experienced severe complications such as contracture. 2. Participants with flexor or extensor tendon injuries of the hand, particularly when accompanied by fractures, will not be eligible for a part in the study. 3. Participants with uncontrolled diabetes or other autoimmune disorders that could interfere with the healing process will be excluded from the study. 4. Participants planning for secondary surgery due to tendon adhesion will be excluded from the study. 5. Participants presenting with fever, swelling, non-healing wounds, open, inflamed, or infected skin surfaces or a tendency to bleed will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
1. Range of Motion- hand and fingerTimepoint: 1. Range of Motion- hand and finger- measure in degrees Time points: pre-intervention and post-intervention, assessed over two weeks.

Secondary

MeasureTime frame
1. Hand function: Action research arm test. 2. Pain: Numeric pain rating scale Time points: pre-intervention and post-intervention, assessed over two weeks.Timepoint: 1. Action Research arm test-score 0-57 2. Numeric pain rating scale- score 0-10 Time points: pre-intervention and post-intervention, assessed over two weeks.

Countries

India

Contacts

Public ContactDr Peeyoosha Gurudat

KLES Institute of Physiotherapy Belgaum

peeyooshagurudut@klekipt.edu.in9844821355

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026