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Clinical Trials/NCT05730868
NCT05730868CompletedNot Applicable

Effect of Exercise Among Turtle Neck Syndrome in Pakistani Patients

University of Karachi1 site in 1 country100 target enrollmentStarted: April 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
The tissue hardness assessed by Algometer measured in Newtons

Study Overview

Brief Summary

Turtle neck also known as Text neck or anterior head syndrome is an overuse syndrome which occurs due to repetitive stress to neck, either by hanging it down or forward using phone or electronic devices. Typical signs and symptoms include pain and stiffness in the neck, shoulder pain and increase curvature of spine. It is becoming a global burden as people of almost all ages are getting affected.

The objective of the study is to find out theEffect of Exercise among Turtle Neck Syndrome in Pakistani Population. A total of 100 participants will be included in the study having both males and females. The pain pattern will be assessed by Visual Analog Scale and Posture Grid Assessment tool will be used to assess posture before and after the treatment session.

The study will be divided into three main sections or groups. One group will be treated by myofascial release only while other group will be treated by muscle energy technique for the management of turtle neck syndrome. Third group will receive both MFP and MET exercise. People having neck pain and those who will be willing to participate will be included in the study.

Detailed Description

The participants will be divided into four groups namely group A, B, C and D. Initially all the participants will be assessed by posture grid assessment tool to check their postural deviations. People meeting the inclusion criteria will be recruited. Group A will receive Muscle Energy Technique (MET) exercise, Group B will receive Myofascial release (MFP) therapy, Group C will receive both MFP and MET and group D will receive conventional treatment. Pre and post Visual analog scale (VAS) will be used to check pain scale and posture grid assessment tool to check postural angles .Pre-assessment will be done on day one and post at the last day of session. The total duration of treatment will be four weeks.

Consent will be taken from the patients. Only those patients meeting the inclusion criteria and screening questions will included in the study and those who will be willing to participate.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •both males and females will be included
  • •patients having non specific neck pain
  • •usage of mobile more than six hours
  • •patients willing to participate

Exclusion Criteria

  • •pregnant females
  • •patients having cervical disc bulge or herniation disoriented patients
  • •patients not willing to participate
  • •patients having any deformity

Arms & Interventions

group 1 myofascial release

Experimental

soft tissue release technique to release tension from muscles which relieves pain and increase range of motion

Intervention: myofascial release (Procedure)

group 2 muscle energy technique

Experimental

soft tissue release technique to release tension from muscles which relieves pain and increase range of motion

Intervention: muscle energy technique (Procedure)

group 3 MFR & MET

Experimental

combination of two soft tissue release techniques to release tension from muscles which relieves pain and increase range of motion

Intervention: MFR & MET (Procedure)

group 4 conventional therapy

Experimental

combination of traditional techniques to relieve pain and spasm

Intervention: conventional therapy (Procedure)

Outcomes

Primary Outcomes

The tissue hardness assessed by Algometer measured in Newtons

Time Frame: 2 years

For tissue hardness, Algometer will be used. It's a device that calculates the hardness when given pressure against the stimuli. The value is measured in Newtons.

visual analog scale

Time Frame: 2 years

For pain intensity visual analog scale will be used. a patient oriented scale ranging from 0-10. 0 means no pain, 1-3 means mild pain, 4-6 means moderate pain and 7-10 means severe pain.

Pain pressure threshold assessed by Algometer measured in Newtons

Time Frame: 2 years

For Pain pressure threshold, Algometer will be used. It's a device that calculates the pain pressure threshold when given pressure against the stimuli. The value is measured in Newtons.

Neck disability Index

Time Frame: 2 years

to check disability, Neck disability Index will be used. It's a ten section questionnaire. Each item has scoring of 0-5. For each section the total possible score is 5. Points are summed to a total score. 0-4points (0-8%) no disability, 5-14points ( 10 - 28%) mild disability, 15-24points (30-48% ) moderate disability, 25-34points (50- 64%) severe disability, 35-50points (70-100%) complete disability

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Khadija Tul Kubra, PT

Assistant Professor

University of Karachi

Study Sites (1)

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