Skip to content

Investigating small blood molecules (miRNAs) as indicators of musculoskeletal pain in runners

Changes in miRNA expression levels following a 6-week kinesiological intervention: a pre-post study in long-distance runners aged at least 35 years

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000120471
Acronym
MiMuS
Enrollment
17
Registered
2025-02-03
Start date
2023-05-30
Completion date
2023-09-30
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

The purpose of this study is to investigate whether a 6-week kinesiological intervention, based on the Canali Postural Method (CPM), can lead to significant changes in the expression of specific microRNAs (miRNAs) in long-distance runners experiencing musculoskeletal pain. The study hypothesizes that the intervention may influence miRNA levels, which could serve as potential biomarkers to monitor musculoskeletal pain and postural balance improvements.

Interventions

The intervention utilizes a kinesiological approach based on the Canali Postural Method (CPM), designed to prevent, reduce, or eliminate compensatory postural patterns by addressing peripheral muscular imbalances, such as resistance or dominance, that may contribute to musculoskeletal pain. Participants follow individualized exercise plans tailored to their specific postural needs. These plans, which emphasize postural adjustments and muscular rebalancing without directly targeting painful areas

The intervention utilizes a kinesiological approach based on the Canali Postural Method (CPM), designed to prevent, reduce, or eliminate compensatory postural patterns by addressing peripheral muscular imbalances, such as resistance or dominance, that may contribute to musculoskeletal pain. Participants follow individualized exercise plans tailored to their specific postural needs. These plans, which emphasize postural adjustments and muscular rebalancing without directly targeting painful areas, are introduced during supervised sessions and reviewed weekly to ensure proper execution and adherence. A CPM-certified operator, trained extensively in CPM techniques, delivers the intervention during one-on-one supervised sessions. The program combines face-to-face supervised sessions with self-managed sessions, allowing participants to practice independently. Exercises are adapted to individual conditions, ensuring pain-free execution or modifications to avoid exacerbating discomfort. The first session also functions as a test phase to identify the origins of compensatory postural patterns and determine appropriate exercises. The intervention consists of alternating sequences of strengthening (e.g. abdominal muscles strengthening) and stretching exercises (e.g. hamstring muscle stretching), repeated in sets. In subsequent sessions, strengthening exercises are progressively increased in duration and difficulty, adjusted according to each participant's capabilities and feedback. The 6-week intervention involves three 60-minute sessions per week, scheduled on non-consecutive days to allow sufficient recovery between sessions. Each week, participants attend one supervised session at the Posture and Movement Laboratory (MP-LAB) of the Institute of Clinical Physiology, while the remaining two sessions are self-managed and conducted in their own training environments.Exercise intensity is dynamically managed during supervised sessions by monitoring participants' ability to maintain proper form while avoiding discomfort or excessive fatigue. Adjustments are made progressively to maintain a balance between challenge and individual capacity.Adherence is monitored during the weekly supervised sessions, where exercise execution is assessed, and feedback is provided to ensure participants remain aligned with the intervention protocol.

Sponsors

National Research Council, Institute of Clinical Physiology, Lecce
Lead SponsorOther

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
35 Years to No maximum
Healthy volunteers
No

Inclusion criteria

long-distance runners registered with Lecce sections of the Italian Federation of Athletics; aged at least 35 years; possession of the medical certificate for competitive sport activity

Exclusion criteria

doctor’s indication not to carry out physical activity during the investigation period; presence of chronic diseases; ongoing pregnancy or less than 6 months from the childbirth and less than 6 months from weaning.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026