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IRCT20220414054537N2 IRCT 2022-07-18 The Superior University effects of mobilization and strength training in patient with forward head posture Comparsion of the effectiveness of mobilization and strength training in improving pain and quality of life in patient with forward head posture 2022-06-10 anticipated 34 Complete https://irct.ir/trial/64304 interventional Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: After baseline assessment patients were divided into two groups A and B randomly by gold fish bowl method. Randomization was done by one of the accessors who was not be a part of research and patient treatment. Randomization assignments was kept in opaque, sealed envelopes and was unsealed by researcher after a baseline treatment. After randomization, the participants in the study was only one to be informed about the allocation of program by the therapist, remaining were unaware of the interventions applied in the other group from may,2022 to july 2022 for two month, Blinding description: the assesor of the study is blind he will not know about the treatment protocol is given to participants and form which group is belongs. N/A Forward head posture (FHP) is a poor habitual neck posture. It often co-exists with Upper Crossed Syndrome. Defined by hyperextension of the upper cervical vertebrae and forward translation of the cervical vertebrae. Intervention 1: Intervention group: the patient will instructed to target one mark corresponding 2 mmHg on the pressure dial at a time. The pressure that will the patient could hold steady for 10 seconds with minimal superficial muscle activity is the one which take as baseline endurance capacity (10 repetitions of 10-second hold). The action will ensure to be pure nod with no head retraction and no head lifting. Subjects will told to perform head nodding action to gradually target and hold the 5 pressure levels for 10 seconds between 22 mmHg and 30 mmHg. The minimum satisfactory performance requirements were 26 mmHg. Each session of consisted of 3 sets, with each set having 10 repetitions. Sessions were performed for a total of 6 weeks with 4 days in a week under the supervision of the therapist for total 8 weeks of the total trial. Intervention 2: Intervention group: Group B will given the mobilization exercises total of three sets will conducted, with one set consisting of repeating the motion that will maintained for 10 s up to 10 times. A break of 5 s will provided per one movement and 30 s per one set. Therefore, the total exercise time will be less <10 min.this treatment will continue for 8 weeks. Yes - There is a plan to make this available What will be shared: All data will be shared aftere de-identification When: data will be avilable when the rial has been completed at the end of the august 2022,the data will be avilable for the future use and after the completeion of trial when it get published approximately after 4 week in the start of of october 2022 and summry of the data will be avilable after the article get published To whom: it will be avilable to all teaching institute and hospital for better care of thepatient more over it will be avilable for the researcher as well Conditions: only for the research and for the benefits of public Where to obtain: the documents will be avilable on the following details email:rehanfaisal68@gmail.com and contact no: +923334816348, the postal address:Department of physical therapy, chaudhary akram teaching hospital the superior university,17 km riwind road,Lahore How to obtain: application sent on the email on request rehanfaisal68@gmail.com Comments:
public Dr Zohaib Shahid
Main Riwind Road 17 km ,Lahore
Lahore Pakistan 54000 +92 333 6979114 Zohaib.rana@superior.edu.pk Committe Azra Naheed Centre for Research & Development the Superior University ,Lahore scientific Dr Zohaib Shahid
Main Riwind Road 17 km ,Lahore
Lahore Pakistan 54000 +92 333 6979114 Zohaib.rana@superior.edu.pk Committe Azra Naheed Centre For Research & Development The Superior University ,Lahore Pakistan Patient with chronic neck pain for more than 3 month Patient with neck disability index less than 24 Patient with prolong sitting workspace enviourment Patient with chronic headache age between 23 to 57 23 years 57 years Both Patient with congenital/acquired postural deformities like scoliosis patient undergone the neck surgeries patient with spinal diseases like compression,tumors,neurological deficits patient with neck fracture and inflammatory disease R29.3 Abnormal posture Rehabilitation Rehabilitation Intervention group: the patient will instructed to target one mark corresponding 2 mmHg on the pressure dial at a time. The pressure that will the patient could hold steady for 10 seconds with minimal superficial muscle activity is the one which take as baseline endurance capacity (10 repetitions of 10-second hold). The action will ensure to be pure nod with no head retraction and no head lifting. Subjects will told to perform head nodding action to gradually target and hold the 5 pressure levels for 10 seconds between 22 mmHg and 30 mmHg. The minimum satisfactory performance requirements were 26 mmHg. Each session of consisted of 3 sets, with each set having 10 repetitions. Sessions were performed for a total of 6 weeks with 4 days in a week under the supervision of the therapist for total 8 weeks of the total trial Intervention group: Group B will given the mobilization exercises total of three sets will conducted, with one set consisting of repeating the motion that will maintained for 10 s up to 10 times. A break of 5 s will provided per one movement and 30 s per one set. Therefore, the total exercise time will be less <10 min.this treatment will continue for 8 weeks. Pain. Timepoint: before the start of the intervention and after the 8 weeks of intervention. Method of measurement: pain will be calculated Numeric pain rating scale. Quality of life. Timepoint: before the start of the intervention and after the 8 weeks of intervention. Method of measurement: The quality of life will be calculated by using Sf-36 quality of life scale. Nil Approved 2022-06-24 committe Azra Naheed Centre for Research & Development the Superior University ,Lahore main riwind road 17 km ,Lahore Lahore Punjab Pakistan