NCT07179133

Brief Summary

Chronic neck pain affects 30-50% of individuals annually and is a leading cause of disability, often linked to muscle imbalances and compensatory over activation of superficial muscles. While craniocervical flexion trainning (CCFT) improves neuromuscular control and reduces pain, limited researches has examined the additional benefits of semispinalis cervicis strengthening. This randomized controlled trial, conducted at Fauji Foundation Hospital and Foundation University College of Physical Therapy will assess the effects of combining semispinalis cervicis strengthening with CCFT on pain, cervical erange of motion, muscle strength and functional disability. Participants will be randomly assigned to either CCFT alone or CCFT with semispinalis cervicis strengthening, performed three times per week for four weeks. Data will be collected at baseline, mid study (week 2) and end of study (week 4) using the Numeric pain rating scale, Goniometer, Sphygmomanometer and Nexk disability index. This study addresses a research gap by exploring deep cervical extensors strengthening alongside CCFT, potentially improving rehabilitation strategies for pain relief, cervical stability and functional recovery.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
6mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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 Progress55%
Sep 2025Nov 2026

First Submitted

Initial submission to the registry

September 11, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 17, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

September 30, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Last Updated

September 23, 2025

Status Verified

September 1, 2025

Enrollment Period

1 year

First QC Date

September 11, 2025

Last Update Submit

September 17, 2025

Conditions

Outcome Measures

Primary Outcomes (4)

  • Chronic Neck Pain

    Chronic Neck Pain will be measured using Numeric Pain Rating Scale, minimum value is 0 and maximum value is 10.

    4 weeks

  • Neck Range of Motion

    Neck Range of Motion will be measured using Goniometer, minimum and maximum value depends on movement.

    4 weeks

  • Neck Muscle Strength

    Neck Muscle Strength will be measured with Sphygmomanometer, minimum and maximm value depends on hold time of 20mmHg.

    4 weeks

  • Neck Functional Disability

    Neck Disability Index will be used to measure Neck Functional Disability, 0 to 50 is range.

    4 weeks

Study Arms (2)

Craniocervical Flexion Training

ACTIVE COMPARATOR

Detailed components of Craniocervical Flexion (CCF) Training

Procedure: Craniocervical Flexion Training alone

Semispinalis Cervicis Strengthening with CCF Training

ACTIVE COMPARATOR

Detailed components of Semispinalis Cervicis Strengthening and Craniocervical Flexion (CCF) Training

Procedure: Semispinalis Cervicis strengthening with Craniocervical Flexion Training:

Interventions

10-minute hot pack treatment before starting the protocol. Week 1: Muscle Activation, • Hold for 5-10 seconds. * Perform in supine with a sphygmomanometer device. * Nod head gently as if saying "yes," aiming for 20-22 mmHg. Week 2: Endurance Training Goal: • Hold for 10-15 seconds. Increase holding time and precision. Exercise: • Maintain the contraction at 24-26 mmHg on the device. Week 3: Strength and Postural Training •Hold for 15 seconds. Exercise: * Perform CCFT in sitting or standing. Week 4: Functional Integration * Maintain contraction during functional tasks (e.g., desk work). * Hold for 15-20 seconds. * Sets/Reps: 3 sets of 8-12 repetitions.

Craniocervical Flexion Training

Craniocervical flexion training will be same as given to group A. Week 1: Semispinalis Cervicis Activation: * Patient sits upright with neutral spine. * Therapist applies gentle manual resistance at C2 vertebra while the patient resists backward motion. * Hold for 3-5 seconds, then relax. Week 2: Progressive Activation with Increased Resistance: * Apply moderate manual resistance at C2. * Hold for 5 seconds, focusing on controlled movement. Week 3: Strength and Functional Coordination with Dynamic Resistance: * Introduce light movement (e.g., slight backward head tilt) under resistance. * Therapist adjusts resistance dynamically. Week 4: Advanced Endurance and Functional Integration with Functional Movements: * Combine resistance training with controlled head rotations or slight lateral flexion. * Maintain resistance and stability. * Reps/Sets: 3-4 sets of 12 reps.

Semispinalis Cervicis Strengthening with CCF Training

Eligibility Criteria

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

You may qualify if:

  • Adults aged 18 to 35.
  • Chronic nonspecific Neck Pain persisting for more than 3 months.
  • Willingness to participate and and signed an informed consent form.
  • Self reported neck pain intensity greater than and equal to 3 on 11 point numerical pain scale.

You may not qualify if:

  • Recent neck injuries and surgeries.
  • Several medical conditions like Hypertension, RA and Cardiovascular Diseases.
  • Significant psychiatric disorders.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Foundation University Islamabad

Islamabad, Punjab Province, 46000, Pakistan

Location

Study Officials

  • Andleeb Zahra

    Foundation University Islamabad

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Andleeb Zahra, DPT

CONTACT

Muhammad Furqan Yaqoob, MS-MSKPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 11, 2025

First Posted

September 17, 2025

Study Start

September 30, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

November 1, 2026

Last Updated

September 23, 2025

Record last verified: 2025-09

Locations