Comparative Effects of Gong's Mobilization With Gradually Graded Exercise Therapy
8 de julho de 2021 atualizado por: Rabiya Noor, Riphah International University
Comparative Effects of Gong's Mobilization With Gradually Graded Exercise Therapy for Chronic Neck Pain Among the Electronic Gadgets Users.
This project was a Randomized clinical trial conducted to find out the Comparative Effects of Gong's Mobilization with Gradually Graded Exercise Therapy for Chronic Neck Pain among the users of Electronic Gadgets so that we can have best treatment option for patients.
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Descrição detalhada
The study design was a Randomized Clinical Trial.
For the study data was collected from sports and spine professionals.
Sample size was calculated with the help of Epitool calculator.
The study will be completed in 6 months duration.
Neck Disability Index (NDI), Numeric Pain Rating Scale (NPRS) for pain intensity and Universal Goniometers for measuring (ROMs) and Forward head posture (FHP) were assessed before and 4 weeks after the treatment through the craniovertebral angle (CVA) measured from a digitized, lateral-view photograph of each subject.
All the subjects were selected using Non Probability convenient sampling technique.
The Subjects were randomly assigned to one of the following two groups: Gong's Mobilization (Group 1) or Gradually Graded Exercise Therapy (Group 2).This study was conducted in accordance with the rules of the Declaration of Helsinki.
Written Informed consent were taken from all the subjects before participating in this trial.
SPSS 25 was used for data entry and analysis.
Tipo de estudo
Intervencional
Inscrição (Real)
28
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Lahore, Paquistão, 54000
- Riphah IU
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Punjab
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Lahore, Punjab, Paquistão, 54000
- Riphah International University
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
15 anos a 65 anos (Filho, Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:• Subjects with an age range of 15 to 65 years having Chronic neck pain for more than 3 months and subjects having a baseline NDI score of atleast 20% (10 points).
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Exclusion Criteria:
• Cervical stenosis
- History of traumatic Injury
- Previous surgery related to cervical spine
- Hypermobility
- Cancer
- Inflammatory rheumatologic diseases
- Severe psychological disorders
- Being pregnant and
- Intervention including exercise or physical therapy in the last 3 months.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Gong's Mobilization
Subjects received gong's mobilization three times in a week for 4 weeks.
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Group A received Gong's mobilization and common treatnent (TENs,Hot pack and cervical stretches).
Gong's mobilization which is concurrent application of Apophyseal joint gliding and end range passive physiological movements while the subject's cervical postures are passively Neutral in order to induce Normal Cervical Extension.
The Subjects in Group A were treated three times in a week for 4 weeks.
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Experimental: Gradually Graded Exercise Therapy
Subjects received gradually graded exercise therapy three times in a week for 4 weeks.
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The Subjects in Group B were received Exercise Therapy and common treatment (TENs, Hot pack and cervical stretches) three times in a week continue for 4 weeks . Each exercise session will take 30 min. It will be consisted of 5 min warm-up exercises, 20 min stabilization exercises, 5 min cool-down, and stretching exercises including neck and shoulder girdle muscles. The aim of Exercise program was to create a neutral spine and activate deep muscles of the cervical spine. The patients were educated to maintain neutral spine during the exercises and throughout the day as much as possible. Scapulothoracic stabilization exercises were included_ specific exercises for the muscles affecting scapular orientation related to neck pain. The subjects were educated to maintain the positions and contractions during the exercises including scapular retraction, eccentric scapular retraction, and combined scapular retraction with shoulder lateral rotation, forward punch, and dynamic hug. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Pain Intensity by 'Numeric Pain Rating Scale'
Prazo: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in pain from baseline was measured at 12th session.
The Numerical Pain Rating Scale (NPRS) is an 11 point pain scale that is completed by subject himself, under the supervision of researcher.
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Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in Neck disability Index 'NDI' score
Prazo: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in Neck disability Index score 'NDI' from baseline was measured at 12th session.
This questionnaire or tool has been designed to give us information as to how neck pain of the subject has affected his/her ability to manage in everyday life.
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Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Cervical Range of Motion (ROM) measured by Universal Goniometer.
Prazo: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in Cervical Range of motion (ROM) from baseline was measured at 12th session.
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Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in Craniovertebral angle CVA measured from a digitized, lateral-view photograph of each subject.
Prazo: Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Change in Craniovertebral angle (CVA) from baseline was measured at 12th session.
Craniovertebral angle (CVA) is a factor that significantly influences pain in those individuals with a forward head posture (FHP).
Craniovertebral angle (CVA) (the angle between the horizontal line passing through C7 and a line extending from the tragus of the ear to C7).
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Baseline (pre treatment readings), Immediate after treatment and post treatment readings( at 4th week)
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
Publicações Gerais
- Celenay ST, Kaya DO, Akbayrak T. Cervical and scapulothoracic stabilization exercises with and without connective tissue massage for chronic mechanical neck pain: A prospective, randomised controlled trial. Man Ther. 2016 Feb;21:144-50. doi: 10.1016/j.math.2015.07.003. Epub 2015 Jul 15.
- Kim DH, Kim CJ, Son SM. Neck Pain in Adults with Forward Head Posture: Effects of Craniovertebral Angle and Cervical Range of Motion. Osong Public Health Res Perspect. 2018 Dec;9(6):309-313. doi: 10.24171/j.phrp.2018.9.6.04.
- Gong W. The effects of cervical joint manipulation, based on passive motion analysis, on cervical lordosis, forward head posture, and cervical ROM in university students with abnormal posture of the cervical spine. J Phys Ther Sci. 2015 May;27(5):1609-11. doi: 10.1589/jpts.27.1609. Epub 2015 May 26.
- McLean SM, Klaber Moffett JA, Sharp DM, Gardiner E. A randomised controlled trial comparing graded exercise treatment and usual physiotherapy for patients with non-specific neck pain (the GET UP neck pain trial). Man Ther. 2013 Jun;18(3):199-205. doi: 10.1016/j.math.2012.09.005. Epub 2012 Oct 22.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
15 de outubro de 2020
Conclusão Primária (Real)
30 de abril de 2021
Conclusão do estudo (Real)
30 de junho de 2021
Datas de inscrição no estudo
Enviado pela primeira vez
26 de março de 2021
Enviado pela primeira vez que atendeu aos critérios de CQ
3 de maio de 2021
Primeira postagem (Real)
4 de maio de 2021
Atualizações de registro de estudo
Última Atualização Postada (Real)
14 de julho de 2021
Última atualização enviada que atendeu aos critérios de controle de qualidade
8 de julho de 2021
Última verificação
1 de julho de 2021
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- REC/Lhr/20/0104
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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