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Effect of Sensory Motor Training for Neck Muscles on Hand Grip Strength in Post-menopausal Fibromyalgia Neck Pain.

28 mai 2026 mis à jour par: Esraa Fikry Massoud, Cairo University
This study will be conducted to investigate the effect of sensory motor training for neck muscles on hand grip strength in post-menopausal fibromyalgia neck pain.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Description détaillée

Fibromyalgia is a chronic disease accompanied by widespread body pain, heightened tenderness in specific anatomical regions, fatigue, sleep disorders, and irritable bowel syndrome.

Prevalence of fibromyalgia is approximately 2-4% in the general population. It predominantly affects 80-90% of women and typically peaks between the ages of 50 and 60.

Post-menopausal fibromyalgia may be attributed to hormonal changes, particularly the decline in estrogen, which plays a role in pain modulation, mood regulation and sleep quality. This hormonal shift, combined with age-related changes in the central nervous system, altered cortisol levels, increased prevalence of psychological comorbidities such as anxiety and depression may contribute to the development or worsening of fibromyalgia symptoms in post-menopausal women.

Neck pain affects about 70-90% of fibromyalgia patients. It can lead to muscle tension, nerve compression, and altered neuromuscular control, particularly affecting the cervical spine and upper limb function. These changes may impair motor output and reduce hand grip strength.

Improving hand grip strength can contribute to better quality of life, functional independence, and may reduce reliance on medication.

Sensory motor training is an emerging rehabilitation approach designed to improve the interaction between sensory input and motor output. It enhances proprioception, coordination, and motor control, which are often impaired in patients with fibromyalgia due to central sensitization and neuromuscular dysfunction.

Sensory motor neck training using laser pointer technique enhances cervical proprioception and motor control in patients with neck pain by providing visual feedback to guide accurate head movements.

So, this study will be conducted to provide new evidences and information about the effect of sensory motor training on hand grip strength in post-menopausal fibromyalgia neck pain to manage this problem upon them and add new information to the field of physical therapy.

Type d'étude

Interventionnel

Inscription (Estimé)

50

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

  • Egypte
      • Cairo, Egypte
        • Esraa Fikry Massoud

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Fifty post-menopausal women clinically diagnosed with fibromyalgia neck pain for more than 3 months.
  • Their age will be ranged from 50-60 years old.
  • Their body mass index (BMI) will be less than 30 kg/m².
  • Their hand grip strength is less than 20 kg for dominant hand as measured by hand-held dynamometer.
  • Their neck pain score is ≥ 4 as measured by the visual analogue scale (VAS).
  • The right hand is the dominant for all of them.

Exclusion Criteria:

  • Participants will be excluded from the study if they have:
  • Recent cervical trauma or surgery.
  • Neurological disorders.
  • Diabetes mellitus.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Neuro dynamic nerve gliding exercises
The participants will receive neuro dynamic nerve gliding exercises in the form of median, radial and ulnar nerve gliding exercises for 50 minutes/session.
Autre: Neuro dynamic nerve gliding exercises
The participants will receive neuro dynamic nerve gliding exercises in the form of median, radial and ulnar nerve gliding exercises for 50 minutes/session (for 15 repetitions, each repetition held for 1-2 minutes with 30 seconds rest intervals between each repetition)
Expérimental: Sensory motor neck training and neuro dynamic nerve gliding exercises
The participants will receive sensory motor neck training using laser pointer technique for 15 minutes/session, 3 times/week for four weeks in addition to neuro dynamic nerve gliding exercises in the form of median, radial and ulnar nerve gliding exercises for 50 minutes/session.
Autre: Neuro dynamic nerve gliding exercises
The participants will receive neuro dynamic nerve gliding exercises in the form of median, radial and ulnar nerve gliding exercises for 50 minutes/session (for 15 repetitions, each repetition held for 1-2 minutes with 30 seconds rest intervals between each repetition)
Autre: Sensory motor neck training

The participants will perform sensory motor neck training by using laser pointer exercise for 15 minutes/session, 3times/ week for four weeks.

  • The laser pointer exercise will be positioned exactly in the center of the participants' forehead and parallel to the ground.
  • Each participant will assume sitting position on comfortable chair at 90cm (about 3 feet) away from the target board (circles shapes), their knees and hips at 90°, their pelvis and low back resting firmly against the back of a chair and their hands resting on their knees.
  • Therapist will be behind the patient and will give her instructions.
  • Align the laser so that it will point straight at the center of the target when the head is in a neutral position
  • at 90 cm away from the target board.
  • The patient will move the head (flexion/extension/rotation), then attempts to return to the starting position
  • Five repetitions will be performed for each movement direction

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Assessment of hand grip strength
Délai: 4 weeks

The hand-held dynamometer (Hoggan Health Industries, Salt Lake City, USA) is an enclosed hydraulic system recording the applied strength in kilograms.

Hand grip strength will be measured for all participants in both groups before and after the end of the study.

Each participant in both groups will be asked to place hand-held dynamometer in her hand, with her arm beside the trunk, the shoulder in a neutral position, the elbow flexed at 90° and to pull the metal bar with her fingers. This procedure will be conducted bilaterally. The mean of three trials for each side (with 3 min resting periods between repetitions to avoid fatigue) will be calculated
4 weeks
Assessment of Disability of the Arm, Shoulder and Hand (DASH)
Délai: 4 weeks

This 30-item tool evaluates symptoms along with physical function, specifically focusing on the level of disability, and offers five response options for each item. Each item offers five response options, spanning from 1, indicating "no difficulty or symptoms present," to 5, indicating "incapable of participating in an activity or experiencing very severe symptoms." Greater score on the DASH indicates increased levels of disability.

The DASH score is used to assess upper limb disability, with higher scores indicating greater impairment. A score of 0 reflects no disability, 1-20 indicates mild disability, 21-40 is moderate, 41-60 is severe, and 61-100 represents very severe disability.
4 weeks
Assessment of neck pressure pain threshold
Délai: 4 weeks

The force dial FDK 20 algometer is a handheld device used to assess the pressure pain threshold (PPT), which is the minimum amount of pressure that induces a sensation of pain. It provides an objective measure of mechanical pain sensitivity in neck.

Each participant will be asked to assume upright position with feet flat, arms relaxed, and neck in a neutral position.

Pressure will be applied perpendicularly to the site of pain at a constant rate of 1 kg/cm² per second.

Each participant will be instructed to indicate when the sensation changed from pressure to the first feeling of pain.

Three readings will be taken at each site with 30-60 seconds rest between trials, and the average will be recorded as the final PPT value
4 weeks
Assessment of pain intensity
Délai: 4 weeks
The visual analogue scale will be used to assess pain intensity. It is a subjective method to determine pain intensity. The scale consists of a 10-centimeter horizontal line, with the left end marked as "no pain" (0) and the right end marked as "worst possible pain" (10).
4 weeks

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Cairo University

Les enquêteurs

  • Chaise d'étude: Azza Nashed, Professor, Cairo University
  • Directeur d'études: Mohamed Kaddah, Professor, Cairo University

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 juin 2026

Achèvement primaire (Estimé)

15 octobre 2026

Achèvement de l'étude (Estimé)

30 octobre 2026

Dates d'inscription aux études

Première soumission

28 mai 2026

Première soumission répondant aux critères de contrôle qualité

28 mai 2026

Première publication (Réel)

3 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

3 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

28 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • P.T.REC/012/00643

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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