In single-handed individuals it is hypothesized that the biomechanical loads are increased due to compensating for the limb loss by increasing force, repetition and by altering postures. Increasing the biomechanical loads, but maintaining the…
ID
Bron
Verkorte titel
Aandoening
Individuals with a congenital or acquired upper limb absence, individuals with brachial plexus injury
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
For the central sensitization protocol the main outcome measures are the Central Sensitization Inventory (CSI) questionnaire and the Quantitative Sensory Testing (QST) outcome measures. The primary outcome measures for the movement protocol are muscle fatigue, upper extremity angles, muscle activity and force.
Achtergrond van het onderzoek
Musculoskeletal complaints (MSC) are highly prevalent among the general population. However, single-handed individuals, due to upper limb absence (ULA) or brachial plexus injury (BPI), are even more prone to the occurrence of MSCs. Development of MSCs may be explained by an imbalance between the biomechanical capacity, which is the anatomical and physical exertion that the body can endure without sustaining damage, and the loads put on the tissues in order to perform a functional activity. Performing activities single-handed or with the help of the remnant limb, with or without wearing a prosthesis, leads to a transfer of the loads to the remaining body structures. This increases force and repetition and may result in muscle fatigue, which can be determined with electromyography (EMG). Another way to compensate for the loss of a limb is by using alternative movement strategies and adjusted postures, which can be measured with kinematics. Another explanation for the development of MSC in this population is the presence of central sensitization. When the central nervous system becomes sensitized, the status of nociceptive neurons are changed, resulting in hypersensitivity, hyperalgesia, allodynia, temporal summation and expansion of painful areas. This study aims to investigate the biomechanical imbalance and presence of central sensitization to aid in the development of new/better treatment plans to prevent and to treat MSC. With this pilot study, imbalance and central sensitization outcomes are specified and identified for these populations. These results can be used in defining future research to further establish relationships.
The overarching aim of this project is to study the factors contributing to MSC in individuals with one functional hand. The two primary objectives are: (P1) to examine the presence of muscle fatigue, caused by imbalance between biomechanical loads and biomechanical capacity, in individuals with ULA or BPI and two-handed controls, and (P2) to examine the presence of central sensitization in individuals with ULA or BPI and two-handed controls. The secondary objectives are: (S1) to examine the effect of prosthesis use on the presence of muscle fatigue in individuals with ULA. (S2) To establish population specific results, to aid in the sample size calculations and methodology of future research.
Doel van het onderzoek
In single-handed individuals it is hypothesized that the biomechanical loads are increased due to compensating for the limb loss by increasing force, repetition and by altering postures. Increasing the biomechanical loads, but maintaining the biomechanical capacity, leads to an imbalance which is hypothesized to lead to a higher prevalence of MSC in single-handed individuals. Additionally, it is hypothesized that single-handed individuals experience more nociplastic pain due to central sensitisation and that therefore the prevalence of MSC is increased.
Onderzoeksopzet
After METC approval, we want to start in Januari 2020. We start with including participants with ULA and BPI, to each patient we an able bodied control on age and gender. The measurements are expected to be completed within a year.
Onderzoeksproduct en/of interventie
A central sensitisation protocol with the Central Sensitization Inventory (CSI) questionnaire and the Quantitative Sensory Testing (QST). And a movement protocol consisting of maximum voluntary contractions (MVC) measurements, the Jebsen Taylor Hand Function Test (JTHFT) and the Functional Capacity Evaluation for One-Handed individuals (FCE-OH).
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Aged 18 and older
- Able to give written informed consent
- Able to read/understand Dutch or English
- All questions of the Physical Activity Readiness Questionnaire (PAR-Q) answered with “no”, and therefore assuming that executing physical activities is reasonably safe.
Specific criteria per subgroup:
- Upper limb absence (ULA): defect at transhumeral, transradial, elbow disarticulation or wrist disarticulation level, so the maximum voluntary contraction (MVC) protocol as part of the movement protocol can be executed.
- Brachial plexus injury (BPI): a score between 0 and 8 on the questionnaire about functional movements of the hand, meaning almost no function of the hand.
- In case of acquired ULA or BPI: ≥ 1 year after amputation or injury
- Able bodied controls: matching based on gender and age group (+ or – 5 years)
- MSC: answered with “yes” on the first two questions about MSC in the questionnaires for the participants. Having complaints like pain, stiffness and tingling of the muscles, bones, nerves and/or joints that are NOT the result of an accident, an infection, a sport injury or a joint disease, occurring for at least four weeks in the past year.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Incapacity to follow instructions
- Manifest co-morbidity, other than MSC, leading to restrictions in physical or mental functioning that interfere with the measurement results. Examples: fractures of the upper extremity bones, muscle dystrophies or stroke.
- Lower extremity complaints, otherwise the legs cannot be used as reference test site in the Quantitative Sensory Testing (QST)
Specific criteria per test:
- QST: signs or suspicion of neurological dysfunction at tested sites
- Capacity tests: history of medical disorder that influence heart rate or use of medication that influences heart rate (for example beta-blockers)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL8001 |
Ander register | METC UMC Groningen : 2019/495 |