Pan African Clinical Trials Registry
South African Medical Research Council, South African Cochrane Centre
PO Box 19070, Tygerberg, 7505, South Africa
Telephone: +27 21 938 0506 / +27 21 938 0834 Fax: +27 21 938 0836
Email: pactradmin@mrc.ac.za Website: pactr.samrc.ac.za
Trial no.: PACTR202008579448288 Date of Approval: 28/08/2020
Trial Status: Registered in accordance with WHO and ICMJE standards
TRIAL DESCRIPTION
Public title Effect of SNAG mobilization on different cervical angles in patient with flattening cervical curve
Official scientific title Effect of SNAG mobilization on different cervical angles in patient with flattening cervical curve
Brief summary describing the background and objectives of the trial The correction sagittal cervical curve has been shown to be an important clinical outcome of health care. Conservative methods to restore or improve cervical lor-dosis are rare. Mulligan pioneered specific manual approach called mobilization with movement (MWM).The advance of this approach was aimed for application on the spinal joints. The most commonly used Mulligan technique is called “sustained natural apophyseal glides” or SNAGs, this technique has introduced in 1999 by Mulligan and is per- formed by applying an accessory glide along the axis of the facet joint of the affected level while the patient is doing an active movement from weight-bearing position. A according to our knowledge, there is no clinical trials investigated the efficacy of mulligan on different sagital cervical alignment in apteient with flattening cervical curve, so this study will conducted to determine the effect of mulligan concept SNAG on different cervical angles on patient with flattening cervical curve
Type of trial RCT
Acronym (If the trial has an acronym then please provide)
Disease(s) or condition(s) being studied Musculoskeletal Diseases
Sub-Disease(s) or condition(s) being studied
Purpose of the trial Rehabilitation
Anticipated trial start date 01/09/2020
Actual trial start date 01/09/2020
Anticipated date of last follow up 01/11/2020
Actual Last follow-up date 05/01/2021
Anticipated target sample size (number of participants) 20
Actual target sample size (number of participants)
Recruitment status Completed
Publication URL
Secondary Ids Issuing authority/Trial register
STUDY DESIGN
Intervention assignment Allocation to intervention If randomised, describe how the allocation sequence was generated Describe how the allocation sequence/code was concealed from the person allocating the participants to the intervention arms Masking If masking / blinding was used
Parallel: different groups receive different interventions at same time during study Randomised Simple randomization using a randomization table created by a computer software program Sealed opaque envelopes Open-label(Masking Not Used)
INTERVENTIONS
Intervention type Intervention name Dose Duration Intervention description Group size Nature of control
Control Group conventional treatment 3 session per week for one month 4 weeks hot packs, stretching exercise and strengthening exercise 10 Active-Treatment of Control Group
Experimental Group SNAG mobilization 3 session per week for one month 4 weeks SNAG mobilization at C5, C6,C7 level for 10 repetition at each level plus conventional treatment 10
ELIGIBILITY CRITERIA
List inclusion criteria List exclusion criteria Age Category Minimum age Maximum age Gender
Patient with flattening cervical curve c2-c7 angle below 20.Patients with mechanical for more than 3 months. A An average cervical pain intensity of 5 or more on a visual analog scale (VAS) (scored out of 10). Their age ranged from 18-30 years old. if they had undergone postural control training, physical therapy during the preceding 12 months, or spinal surgery; complained of any neurological signs; had any history of cervical spine disc herniation or cervical trauma; were pregnant; had congenital postural deformities; or exhibited a definitive visual disorder Adolescent: 13 Year-18 Year,Adult: 19 Year-44 Year 18 Year(s) 30 Year(s) Both
ETHICS APPROVAL
Has the study received appropriate ethics committee approval Date the study will be submitted for approval Date of approval Name of the ethics committee
Yes 15/07/2020 faculty of physical therapy research ethics
Ethics Committee Address
Street address City Postal code Country
7 Ahmed EL Zayad street,Dooki, Giza, Egypt Giza 12612 Egypt
OUTCOMES
Type of outcome Outcome Timepoint(s) at which outcome measured
Primary Outcome different cervical angles c2-c7, c1-c2, oc-c2 angles pre and post treatment
Secondary Outcome neck disability index pre and post treatment
Secondary Outcome visual analogue scale pre and post treatment
RECRUITMENT CENTRES
Name of recruitment centre Street address City Postal code Country
faculty of physical therapy 7th el zayat street Giza 12612 Egypt
FUNDING SOURCES
Name of source Street address City Postal code Country
Mariam Omran Grase 7 Ahmed ElZaiat St. Ben Elsaryat ElDokki Giza 12612 Egypt
SPONSORS
Sponsor level Name Street address City Postal code Country Nature of sponsor
Primary Sponsor Mariam Omran Grase 7 Ahmed ElZaiat St. Ben Elsaryat ElDokki Giza 12612 Egypt Individual
COLLABORATORS
Name Street address City Postal code Country
Al Shaymaa Shaaban Abdelazeim 7 Ahmed El Zaiat St. BenElsaryat El Dokki Giza 12612 Egypt
CONTACT PEOPLE
Role Name Email Phone Street address
Principal Investigator Mariam Grase dr.mariamomran@gmail.com 00201281940603 7 Ahmed Elzaiat St.BenElsaryat
City Postal code Country Position/Affiliation
Giza 12612 Egypt lecturer
Role Name Email Phone Street address
Public Enquiries Mariam Grase dr.mariamomran@gmail.com 0020281940603 7 Ahmed Elzaiat St.BenElsaryat EI Dokki
City Postal code Country Position/Affiliation
Giza 12612 Egypt Lecturer
Role Name Email Phone Street address
Scientific Enquiries al shaymaa shaaban alshaymaa.shaaban@pt.cu.edu.eg 01033771553 7th el zayat street
City Postal code Country Position/Affiliation
Giza 12612 Egypt Lecturer
REPORTING
Share IPD Description Additional Document Types Sharing Time Frame Key Access Criteria
Yes 20 patients have flattening cervical curve from both sexes.this patient will be assessed by vas, neck disability and Xrays for different cervical angles Study Protocol beginning 3 months and ending two year following article publication the criteria will be accessed by the publication of trials in international journa
URL Results Available Results Summary Result Posting Date First Journal Publication Date
No
Result Upload 1: Result Upload 2: Result Upload 3: Result Upload 4: Result Upload 5:
Result URL Hyperlinks Link To Protocol
Result URL Hyperlinks
Changes to trial information