Effect of Instrument-assisted Soft Tissue Mobilization on Functional and Cognitive Abilities in Elderly
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Instrument-assisted soft tissue mobilization, Traditional physical therapy.
- Who it may be relevant to
- Registry conditions: Functional Abilities, Cognitive Abilities. Basic parameters: 65 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
PURPOSE: To determine the effect of Instrument-assisted soft tissue mobilization on functional and cognitive abilities in elderly. BACKGROUND: There is an increased interest in health care with growth of the older population. Instrument-Assisted Soft Tissue Mobilization (IASTM) is a manual therapy technique using specially designed tools to apply pressure and mobilize soft tissues. It has gained attention as a non-invasive intervention that can aid in improving musculoskeletal health and overall function, especially in older adults. Given the aging population and the rise in age-related functional and cognitive decline, there is a pressing need for effective strategies to enhance quality of life in this demographic. In the elderly, musculoskeletal issues, such as reduced muscle flexibility, joint stiffness, and soft tissue restrictions, are common and can severely impact physical function. IASTM has been shown to increase tissue perfusion, reduce fascial restrictions, and improve joint mobility. These effects are critical in countering age-related declines in mobility, balance, and overall physical functionality, ultimately promoting greater independence and reducing fall risk. Improved physical function through IASTM may also influence cognitive health positively, as increased physical activity and mobility are linked to better cognitive outcomes in the elderly. HYPOTHESES: There will be no significant effect of Instrument-assisted soft tissue mobilization on functional and cognitive abilities in elderly. RESEARCH QUESTION: Does instrument-assisted soft tissue mobilization is effective on functional and cognitive abilities in elderly?
Interventions
- Device Instrument-assisted soft tissue mobilization
IASTM will be delivered using stainless-steel instruments with beveled edges, applied to the target muscle groups for approximately 20 minutes per session, two times per week, over four weeks. A licensed physical therapist trained in IASTM will perform the procedure. Lubricant will be applied to the skin, and strokes will be delivered in multiple directions with pressure adapted to patient tolerance. - Behavioral Traditional physical therapy
The control group will receive a traditional physical therapy program focusing on strength, balance, flexibility, and functional mobility training, combined with simple cognitive stimulation tasks. Sessions will last 30 minutes, two times per week, for four weeks, supervised by a licensed physical therapist.
Primary outcome measures
- Change in Short Physical Performance Battery (SPPB) score [Time frame: Baseline and 4 weeks (end of treatment).]
Secondary outcome measures (1)
- Change in Montreal Cognitive Assessment (MoCA) score [Time frame: Baseline and 4 weeks (end of treatment).]
Eligibility criteria
Inclusion criteria
- 60 elderly subjects aged range from 65-75 years old will participant in the study from both genders.
- had cognitive abilities to understand explanations and instructions
- did not take any medication that can affect their balance.
Exclusion criteria
- They neither had sever musculoskeletal disorders
- Nor neurological damage related to balance (dizziness, vestibular dysfunction)
- Nor orthostatic hypotension
- Nor health risk factors.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Faculty of physical therapy — Giza
Identifiers
NCT: NCT07208630 · P.T.REC/012/005610