- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT05258240
Effects of Virtual Reality-based Balance Training on Balance of Diabetic Peripheral Neuropathy Patients
A Randomized Controlled Trial On The Effects Of Virtual Reality-Based Balance Training On Balance In Patients With Diabetic Peripheral Neuropathy
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
A randomized control trial will be conducted at the study setting Safi Hospital Faisalabad after the approval of the synopsis. The study will be a single-blinded randomized control study. A convenient sampling technique will be used for the enrollment of the patient. Patient selection will be done based on defined insertion and omission criteria.
Two groups would be made, the intervention group would receive the virtual gaming exercise tutoring and the control group would receive the regular physiotherapy exercises.
The evaluation of the patients will be done at the start of the study, after six weeks, and after twelve weeks. Follow-up will be in the 16th weeks after the cessation of therapy.
The patient's outcome will be measured on Berg Balance Scale and the Single Leg Stance test and the patient's data will be recorded before and after treatment, comparisons between before the treatment and after the treatment data will be made after 12 weeks. Informed consent/approval would be taken from each patient. Analysis and entry of data will be done by Statistical Package of Social Sciences Version 22 Software.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Punjab
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Faisalabad, Punjab, Pakistan, 38000
- Ripah International University
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Adults age (45-65 years)
- Male and female (both gender)
- Medical diagnoses of type-II diabetes
- DPN confirmed by physician
- Stages ( Ia - sign but no symptoms of neuropathy, Ib - symptomatic mild diabetic poly neuropathy, sensory, motor or autonomic symptoms; patient able to heel walk)
- Patients independent in transfer.
- Unimpaired cognition/intelligence (Mini Mental State Examination Score of >24)
Exclusion Criteria:
- Any neurological diseases e.g. Dementia, Parkinson, Stroke
- Severe visual impairment and Cardiopulmonary disease
- Musculoskeletal disorder, any disease due to individual were unable to walk and lower limb amputation
- Disease which has chances of falling
Plan d'étude
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 |
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Autre: Virtual Reality
Virtual reality workout session will be for about 50 minutes in which warm-up exercise will be for 5 minutes including relaxed breathing, selected exercises for dynamic balance and static balance will take 40 minutes of the session in which games; tilt city, soccer heading, table tilt game, and penguin tilt will be used for dynamic balance training.
For static balance training games will be torso leg curl and single leg extension.
After that 5 minutes will be given for cools down.
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Virtual reality workout enhances balance control, self-reported balance and mental stability in healthy and stable adults.
Sensory-based exercise and the response to visual acuity can increase the patient's ability to maintain their body in a stable position.
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Autre: Conventional Physical Therapy
Conventional physical therapy will be provided to this group for 50 minutes, with one minute of rest for every five minutes of exercise.
Warm-up for 5 minutes, balancing-drills for 40 minutes, and cools down for five minutes.
The session will include; slow and deep breathing exercise for about 3 minutes, patient will be asked to move both ankle joint to its complete range of movement for about five minutes, posture training for balance includes standing from sitting for five times, shifting the weight of the body while standing at one place for five times, move the body to the side and forward to aim the objective set by the therapist for five times, lift or raise the heels for five times of both foot for 20 seconds for each rise, to stand on one foot for 15 seconds, five times, to stand on one foot and bend the knee for about 15 seconds, five times.
Wobble board preparation gait training and spot marching will be performed for about 5 to 6 minutes each.
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Postural training, standing, walking, and walking activities are included in the conventional physical therapy in domain of balance exercise training programs.
These activities are usually boring and tedious because these exercises are repeated many times.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Berg balance scale
Délai: 12th Week
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The Berg Balance Scale is used to objectively determine a patient's ability or inability to safely balance during a series of predetermined tasks.
Berg Balance Scale (BBS) is a 14-item objective measure that assesses static balance and fall risk in adults.
Berg balance scale scoring ranges from 0 to 56.
The lower your score, the more at risk you are for losing your balance.
In general, Berg balance scale scores are interpreted as such: 0 to 20: A person with a score in this range will likely need the assistance of a wheelchair to move around safely.
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12th Week
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Single leg standing test
Délai: 12th Week
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Single leg standing test used to assess static postural and balance control.
... Client must stand unassisted on one leg, timed from the time the other foot leaves the ground till when the foot touches the ground again or the arms leave the hips.
Participants unable to perform the one-leg stand for at least 5 seconds are at increased risk for injurious fall.
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12th Week
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Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- REC-FSD-00296
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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