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Completed

NCT Number: NCT07403344

Comparative Effects of Sahrmann and Kendall Exercises in Patients With Text Neck Syndrome.

The study was conducted to determine the comparative effects of Sahrmann and Kendall exercises on pain, range of motion and disability in patients with text neck syndrome.

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

PulseCore Physio and Rehab Centre

Lahore, Punjab Province, 54000, Pakistan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged from 18 to 35 years
  • Both male and female were included.
  • Participants who used smartphone for more than 2 hours daily
  • Participant with neck pain aggravated by sustained posture, stiffness on neck and neck turning, the Craniovertebral angle (CVA) <50°
  • Participant with rounded shoulder angle (RSA) greater than 52° (51)
  • Participants with pain greater than 5 on numeric pain rating scale (NPRS)
  • Participants with neck disability index (NDI) of >10

Exclusion criteria

  • • Participants with any spinal infection example: osteomyelitis
  • Participant with any inflammatory condition example: rheumatoid arthritis
  • Participant with any previous cervical surgery
  • Traumatic injury
  • Torticollis, and scoliosis or any pregnant females
  • Participant with any disc prolapse or other spinal issues like stenosis, herniation of disc, spondylolisthesis and osteoporosis
  • Participants taking pain related medication or have gone under physical therapy sessions
  • Participant with Malignancy

Treatment and study plan

Sahrmann exercise

Other

Sahrmann exercises which include Deep Neck Flexor Activation (Chin Tucks), Cervical Flexion with Scapular Stabilization, Shoulder Blade Retractions, Controlled Cervical Rotations, Scapular Depression with Resistance Bands, Neck Flexion Isometric, Cervical Side Bending with Resistance, Thoracic Extension Exercises. Each containing 5 repetitions, each held for 5-10 seconds, Total 3 sessions per week for 4 weeks.

Kendall exercise

Other

Kendall exercise includes Deep Neck Flexor Activation (supine chin tucks) for 2 to 8s, stretch cervical extensors, Scapular Retraction with resistance, Pectoralis major and minor stretch. Each posture was maintained for 30s and 6 sets of 12 repetitions were performed with 3 sessions per week on alternate days for 4 weeks.

standard physical therapy treatment

Other

Both groups were given Standard Physical Therapy treatment including hot pack (applying a moist heat pack to the neck for 7-10 minutes, relaxing muscles, and alleviating pain. Use a towel as a barrier to avoid burns.) and Soft Tissue Mobilization Protocol (involves applying targeted pressure to neck muscles, releasing tension and improving circulation. Additionally, postural education focused on maintaining an upright posture while using mobile devices. This involved holding the device close to eye level and using it while either standing or sitting. Repeat 2-3 times daily for 4 weeks.

Primary outcomes

  1. Numeric Pain Rating Scale

    Time frame: From enrollment to the end of treatment at 4 weeks

    The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

  2. Neck Disability Index

    Time frame: From enrollment to the end of treatment at 4 weeks

    Neck pain disability index is used for the disability of the neck or the impact of neck pain on a person. This 10-item questionnaire is used to assess the patient overall quality of life as well as the personal ability to perform activities of daily living. It has various categories ranging from personal care, lifting, reading etc. it has a scoring range from zero disability. The greater the scored the higher the disability of neck.

Secondary outcomes

  1. ROM Cervical Spine (Flexion)

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine flexion ROM at baseline and 4th week of intervention was measured using goniometer.

  2. ROM Cervical Spine (Extension)

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine extension ROM at baseline and 4th week of intervention was measured using goniometer.

  3. ROM Cervical Spine (Lateral Flexion) Left Side

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine Lateral flexion on left side ROM at baseline and 4th week of intervention was measured using goniometer.

  4. ROM Cervical Spine (lateral Flexion) Right Side

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine lateral flexion on right side ROM at baseline and 4th week of intervention was measured using goniometer.

  5. ROM Cervical Spine (Rotation) Left Side

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine rotation on left side ROM at baseline and 4th week of intervention was measured using goniometer.

  6. ROM Cervical Spine (Rotation) Right Side

    Time frame: From enrollment to the end of treatment at 4 weeks

    Changes in cervical spine rotation on right side ROM at baseline and 4th week of intervention was measured using goniometer.

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Comparative Effects of Sahrmann and Kendall Exercises on Pain, Range of Motion and Disability in Patients With Text Neck Syndrome.

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 11, 2026
Registry last updated
Feb 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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