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Soft Tissue Injury Rehabilitation

Optimizing Soft Tissue Injury Rehabilitation PEACE & LOVE Concept with Cryotherapy vs Without Cryotherapy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073357
Enrollment
46
Registered
2024-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: M709- Unspecified soft tissue disorder related to use, overuse and pressure

Interventions

Intervention1: Cryotherapy and the PEACE & LOVE concept: For acute soft tissue injury, this group will receive the PEACE & LOVE protocol, beginning on the first day of the injury and continuing throug

Sponsors

Polok Halder
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to participate, participants need to fulfill the following requirements: (1a) Acute soft tissue injury, such as sprains, strains, contusions, or minor lacerations. (1b) symptoms such as warmth or tingling in the area of the injury, pain, swelling, bruising, restricted range of motion, tenderness, weakness, stiffness, instability, and (1c) injuries that occurred within the last 48 hours. The following additional requirements are also included: (2) Between the ages of 20 to 30 (3) Any gender (4) A Severity score of 1–8 on the Visual Analogue Scale (VAS), and (5) Willingness to follow to the prescribed treatment plan and follow-up evaluations. (6) Understanding and providing informed consent.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they have: (1) Chronic soft tissue injuries or conditions. (2) Age not in the range of between 20 and 30 years old. (3) Severe soft tissue injuries that need to be operated on right away. (4) Not being able to understand or give informed consent. (5) Concurrent illnesses or injuries that might affect the results or call for different treatment approaches. (6) Any conditions, such as allergies or recent negative reactions, that would restrict the treatments described in both protocols.

Design outcomes

Primary

MeasureTime frame
Pain in NPRS scaleTimepoint: 7 days

Secondary

MeasureTime frame
Physical Functional Stutas in the physical function measures of SF-36Timepoint: 7 days;Recovery time in calculating the difference between the date of injury and the date of recoveryTimepoint: 7 days;Swelling in Figure-of-eight measurementTimepoint: 7 days

Countries

Bangladesh

Contacts

Public ContactDr K M Amran Hossain

Jashore University of Science and Technology

mz.hossain@just.edu.bd01670962775

Outcome results

None listed

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