NCT07042230

Brief Summary

Mechanical neck pain is a common musculoskeletal condition that affects many people, especially those with poor posture or repetitive neck movements. It can cause discomfort, reduce the ability to move the neck, and affect daily functioning. This study aimed to compare the effects of two physiotherapy treatments-Proprioceptive Neuromuscular Facilitation (PNF) and Passive Vertebral Mobilization (PVM)-on neck pain, disability, and movement. This randomized controlled trial was conducted at the University of Lahore Teaching Hospital over nine months. A total of 62 participants, aged 18 to 35 years, who had mechanical neck pain for at least four weeks, were recruited and randomly assigned to one of two groups: Group A received PNF, while Group B received PVM. Both treatments were delivered by physiotherapists three times per week for four weeks. PNF is an active therapy that involves specific movement patterns to improve muscle coordination and flexibility. PVM is a passive manual therapy technique where the therapist gently moves the neck vertebrae to improve joint mobility and reduce pain. Outcomes were measured using the Neck Disability Index (NDI), the Numeric Pain Rating Scale (NPRS), and measurements of neck movement (Active Cervical Range of Motion, or ACROM) at the start of the study, at two weeks, and at the end of the four-week treatment. The study was single-blinded-meaning the person assessing the outcomes did not know which treatment the patient received. The results showed that both treatments significantly improved pain, movement, and function. However, the group that received PNF showed slightly greater reduction in pain scores by the end of the treatment. There were no significant differences between the groups in terms of disability or movement range. This study concluded that both PNF and PVM are beneficial treatments for mechanical neck pain. PNF may offer slightly faster pain relief, while both interventions are effective at improving mobility and reducing neck-related disability. These findings can help guide physiotherapists and patients in choosing suitable treatment options for neck pain.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2024

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 17, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 16, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 6, 2025

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

June 18, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 27, 2025

Completed
Last Updated

June 27, 2025

Status Verified

June 1, 2025

Enrollment Period

8 months

First QC Date

June 18, 2025

Last Update Submit

June 26, 2025

Conditions

Keywords

ArticularCervical VertebraeManual TherapyNeck PainProprioceptionRange of Motion

Outcome Measures

Primary Outcomes (1)

  • Neck Disability

    The Neck Disability Index (NDI) is a validated, self-reported questionnaire that assesses disability related to neck pain. It contains 10 items, each scored from 0 to 5, with higher scores indicating greater disability. The total score ranges from 0 to 50 and is converted into a percentage. This outcome will assess improvement in neck-related function and disability following 4 weeks of intervention with either PNF or PVM.

    Baseline, Week 2, and Week 4

Secondary Outcomes (2)

  • Cervical Pain

    Baseline, Week 2, and Week 4

  • Active Cervical Range of Motion (ACROM)

    Baseline, Week 2, and Week 4

Study Arms (2)

Proprioceptive Neuromuscular Facilitation (PNF)

EXPERIMENTAL

Participants in this arm received Proprioceptive Neuromuscular Facilitation (PNF) techniques aimed at improving neck mobility, pain, and function. The intervention included rhythmic initiation, dynamic reversals, and contract-relax techniques performed across four cranio-cervical diagonal movement patterns (e.g., extension with left rotation, flexion with right rotation). Each session lasted 15-30 minutes and was delivered three times per week for four weeks. Techniques were progressed based on patient tolerance, with repetitions increased in the third and fourth weeks. All sessions were administered by licensed physiotherapists following standardized protocols.

Other: Proprioceptive Neuromuscular Facilitation (PNF)

Passive Vertebral Mobilization (PVM)

EXPERIMENTAL

Participants in this arm received Maitland-based Passive Vertebral Mobilization (PVM) techniques targeting cervical vertebrae to improve joint mobility and reduce neck pain. Mobilizations were applied in prone lying using posteroanterior central and unilateral glides. Treatment began with Grades I-II oscillatory mobilizations in Weeks 1-2, progressing to Grades III-IV in Weeks 3-4, based on patient response and tolerance. Each session lasted 15-20 minutes and was conducted three times per week for four weeks. Interventions were performed by trained physiotherapists using standardized procedures.

Other: Passive Vertebral Mobilization (PVM)

Interventions

Proprioceptive Neuromuscular Facilitation (PNF) techniques were applied to the cervical region using rhythmic initiation, dynamic reversals, and contract-relax methods. Movements followed diagonal cranio-cervical patterns including flexion/extension with rotational components. Each session lasted 15-30 minutes, delivered three times per week for four weeks. Repetitions and sets were progressively increased based on patient tolerance. The goal was to enhance neuromuscular coordination, improve cervical range of motion, and reduce pain through active facilitation techniques.

Also known as: PNF Stretching, PNF Cervical Patterns
Proprioceptive Neuromuscular Facilitation (PNF)

Passive Vertebral Mobilization (PVM) was administered using Maitland mobilization techniques applied to the cervical spine. Posteroanterior central and unilateral glides were performed with the participant in a prone position. Mobilizations started with Grades I-II during Weeks 1-2 and progressed to Grades III-IV in Weeks 3-4, depending on patient response. Each session lasted 15-20 minutes and was conducted three times weekly over four weeks. This passive manual therapy aimed to improve joint mobility, reduce muscle stiffness, and alleviate mechanical neck pain.

Also known as: Cervical Maitland Mobilization, Spinal Mobilization Techniques
Passive Vertebral Mobilization (PVM)

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Participants aged between 18 and 35 years were included in the study (Ashfaq et al., 2022).
  • Participants diagnosed with pain localized in the neck region for at least 4 weeks were included.
  • Participants diagnosed with no radiating pain beyond the shoulder or fingers were included (Cohen, 2015).
  • Participants diagnosed with no identified neurological deficits were included.
  • Participants having no history of major trauma or surgery to the cervical spine were included (Rodríguez-Huguet et al., 2020).

You may not qualify if:

  • Participants who were diagnosed with ankylosing spondylitis, rheumatoid arthritis, fracture of spine, cancer or congenital anomaly of the cervical spine, positive neurological findings (Ashfaq et al., 2022).
  • Patients with any other contraindication to manual therapy (Ashfaq et al., 2022).
  • Neurological conditions affecting the cervical spine.
  • Uncontrolled dizziness or vertigo (Cohen, 2015).
  • Known malignancy or any pregnancy (Cohen, 2015).
  • Current use of medications that could affect pain perception (e.g., opioids, high-dose antidepressants) (Rodríguez-Huguet et al., 2020)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of Lahore Teaching Hospital

Lahore, 54590, Pakistan

Location

MeSH Terms

Conditions

Neck Pain

Interventions

Muscle Stretching Exercises

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist

Study Record Dates

First Submitted

June 18, 2025

First Posted

June 27, 2025

Study Start

August 17, 2024

Primary Completion

April 16, 2025

Study Completion

June 6, 2025

Last Updated

June 27, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations