NCT07048288

Brief Summary

Exercises are widely regarded as the primary approach for managing cervical spondylosis. Although several studies have examined the effectiveness of multi-angle isometric exercises and dynamic exercises in patients with cervical spondylosis, their findings have been inconsistent. Further research is warranted to determine whether combining dynamic exercises with Kinesio taping can yield superior therapeutic outcomes. Additionally, there is a lack of comparative studies evaluating the relative benefits of multi-angle isometric versus dynamic exercises for individuals with cervical spondylosis. Therefore, this study aims to compare the efficacy of Multi-angle isometric exercise and Dynamic exercise, along with kinesio taping, in improving range of motion in the cervical spine, reducing pain, and improving functional disability in patients with Cervical Spondylosis. Fifty-two participants were randomly assigned to Experimental Group 1 (EG1) and Experimental Group 2 (EG2), with 26 participants in each group. EG1 received Multi-angle isometrics and Kinesio taping along with conventional physiotherapy, while EG2 received Dynamic exercise and Kinesio taping along with conventional physical therapy. Both groups were treated for 9 weeks. Goniometry and the Neck Pain and disability index were used as outcome measures.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
52

participants targeted

Target at P25-P50 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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 2, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 26, 2024

Completed
23 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2024

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

June 24, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 2, 2025

Completed
Last Updated

September 3, 2025

Status Verified

June 1, 2025

Enrollment Period

7 months

First QC Date

June 24, 2025

Last Update Submit

August 26, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Goniometry

    Goniometry is the measurement of joint angles using a device called Goniometer. Greater joint angles indicate better treatment outcomes.

    Pre-intervention values were taken before the intervention, and post-intervention values were taken in week 10 (after 9 weeks of treatment).

  • Neck Pain and Disability Index

    The Neck Disability Index (NDI) is a self-report questionnaire designed to measure how neck pain affects a person's ability to manage daily life. Each section has six statements scored from 0 (no disability) to 5 (maximum disability), with a total possible score of 50. The higher the score, the greater the perceived disability.

    Pre-intervention values were taken before the intervention, and post-intervention values were taken in week 10 (after 9 weeks of treatment).

Study Arms (2)

Experimental Group 1

EXPERIMENTAL

Experimental group 1 received multi-angle isometrics and kinesio taping along with conventional physiotherapy.

Other: Multi-angle isometricsOther: Kinesio tapingOther: Conventional Physiotherapy

Experimental Group 2

ACTIVE COMPARATOR

Experimental Group 2 received dynamic exercise and kinesio taping along with conventional physical therapy.

Other: Kinesio tapingOther: Dynamic exerciseOther: Conventional Physiotherapy

Interventions

Multi angle exercises include cervical flexion training, Cervical extension training, and Cervical lateral flexion training

Experimental Group 1

Kinesio taping is a therapeutic technique used in rehabilitation to support muscles and joints without restricting movement.

Experimental Group 1Experimental Group 2

The dynamic exercise program included dynamic cervical flexion, dynamic cervical extension, and dynamic lateral flexion.

Experimental Group 2

Conventional physiotherapy included transcutaneous electrical nerve stimulation

Experimental Group 1Experimental Group 2

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients diagnosed with Cervical Spondylosis aged between 30 - 50.
  • Both genders.
  • Patients with radiological findings of Cervical Spondylosis confirmed by a medical professional.
  • Patients without any surgical indication.

You may not qualify if:

  • Patients with cervical radiculopathy.
  • Patients with other cervical spine problems such as; a history of fracture or dislocation, ankylosing spondylitis, congenital cervical anomalies, cervical spine stenosis, cervical spondylotic myelopathy, rheumatoid arthritis, bone tumor, and tuberculosis.
  • Patients with pacemakers.
  • Patient with psychiatric conditions.
  • In cases where the Kinesio taping technique is contraindicated, such as thrombosis, wound, intolerability, allergy to tape, or impaired sensation.
  • Patients receiving any form of medications including steroids, NSAIDs or analgesics.
  • Patients who do not have good compliance with the intervention or have difficulty in co-operating with the study.
  • Patients who cannot read or understand English.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

AWH Special College

Calicut, Kerala, 673003, India

Location

MeSH Terms

Conditions

Spondylosis

Condition Hierarchy (Ancestors)

Spinal DiseasesBone DiseasesMusculoskeletal Diseases

Study Officials

  • Khan, MPTh

    King Saud University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: A two-arm parallel-group pre-test-post-test design was used in this randomized controlled trial.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Researcher

Study Record Dates

First Submitted

June 24, 2025

First Posted

July 2, 2025

Study Start

August 2, 2023

Primary Completion

February 26, 2024

Study Completion

March 20, 2024

Last Updated

September 3, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations