NCT06228664

Brief Summary

This study aims to compare the effects of both the therapies on postural changes, pain, decreased ROM, and functional disability among students suffering from Text Neck Syndrome.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2023

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

January 18, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 29, 2024

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2024

Completed
Last Updated

March 5, 2024

Status Verified

March 1, 2024

Enrollment Period

6 months

First QC Date

January 18, 2024

Last Update Submit

March 4, 2024

Conditions

Keywords

text neck syndromeneck painbowen therapyfoam rolling

Outcome Measures

Primary Outcomes (2)

  • Neck Disability Index

    Changes from baseline, The neck disability index is a ten item self-reported questionnaire that assesses pain and associated disability, with a total max score of 50 points

    6 week

  • NPRS

    Changes from baseline.The Numeric Pain Rating Scale (NPRS) measures the subjective intensity of pain. The NPRS is an eleven-point scale from 0 to 10. "0" = no pain and "10" = most intense pain

    6 week

Study Arms (2)

foam rolling

ACTIVE COMPARATOR

foam rolling along with conventional physical therapy treatment

Other: foam rolling

bowen therapy

EXPERIMENTAL

bowen therapy along with conventional physical therapy treatment

Other: bowen therapy

Interventions

Foam Rolling Technique on trapezius and suboccipital muscles.conventional therapy (15 min Hot pack, neck isometric exercises and cervical ROM exercises within pain free range). Patients will be treated 3 times per week for 6 consecutive weeks

foam rolling

Bowen Therapy. conventional therapy (15 min Hot pack, neck isometric exercises and cervical ROM exercises within pain free range) will be given to both groups. Patients will be treated 3 times per week for 6 consecutive weeks

bowen therapy

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • neck-head trauma
  • history of surgical intervention in the neck area
  • neurological deficit
  • severe neck pain which required medical treatment
  • cervical disc disease with radiculopathy
  • inflammatory or malignant type of pain
  • systematic disease
  • scoliosis
  • kyphosis.

You may not qualify if:

  • neck-head trauma
  • history of surgical intervention in the neck area
  • neurological deficit
  • severe neck pain which required medical treatment
  • cervical disc disease with radiculopathy
  • inflammatory or malignant type of pain
  • systematic disease
  • scoliosis
  • kyphosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CECOS university of IT and emerging sciences

Peshawar, KPK, 25000, Pakistan

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Asmar Fatima, MS OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 18, 2024

First Posted

January 29, 2024

Study Start

August 1, 2023

Primary Completion

January 30, 2024

Study Completion

January 30, 2024

Last Updated

March 5, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations