CClinicalTrials.gg
CompletedNCT07546838EIH-CNNPUpdated Apr 23, 2026

Effects of Aerobic and Combined Exercise on Pain and Fatigue in Workers With Chronic Neck Pain

An interventional study of Aerobic Exercise and Combined Exercise in Neck Pain Musculoskeletal and Work Related Musculoskeletal Disorders, sponsored by Hacettepe University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 20 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-04-23.

Sponsored by Hacettepe University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled May 2025, registered Apr 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
78
Allocation
Randomized
Ages
20 Years to 65 Years
Sex
All
01

Study summary

This randomized controlled trial investigated the acute effects of aerobic exercise (AE) and combined aerobic and cervical-upper extremity resistance exercise (CE) on the pressure pain threshold (PPT), pain perception, and fatigue in workers with high ergonomic risk and chronic non-specific neck pain (CNNP).

A total of 78 workers were randomly assigned to AE, CE, or control groups. The AE and CE groups completed single 40-minute sessions, while the control group received a 30-minute educational session with additional seated rest periods before and after the session. PPT was assessed bilaterally at multiple anatomical sites using a digital pressure algometer. Neck pain, overall pain perception, and fatigue were evaluated using a numerical rating scale (NRS) before, immediately after, and 20 minutes after exercise.

The study focused on exercise-induced hypoalgesia (EIH) and was intended to inform brief, workplace-compatible exercise strategies to reduce pain, fatigue, and work-related musculoskeletal risks in this population.

Read the detailed description

This randomized controlled trial investigated the acute effects of aerobic exercise and combined aerobic and cervical-upper extremity resistance exercise on pain sensitivity, pain perception, and fatigue in workers with chronic non-specific neck pain exposed to high ergonomic risk.

Participants were recruited from occupational groups with high ergonomic risk and were assessed in two sessions. The first session was conducted in the workplace and included eligibility screening, demographic data collection, and ergonomic risk assessment. Participants were then randomly assigned to aerobic exercise, combined exercise, or control groups.

The second session was conducted in a university laboratory setting. Baseline assessments were performed, followed by the intervention. Outcome measures were collected before the intervention (T0), immediately after (T1), and 20 minutes after the intervention (T2).

The aerobic exercise group performed moderate-intensity cycling using a recumbent ergometer (64-76% of maximum heart rate), consisting of a 5-minute warm-up, 30 minutes of exercise, and a 5-minute cool-down. The combined exercise group performed aerobic exercise at the same intensity, followed by cervical and upper-extremity resistance exercises focusing on motor control and scapular stabilization. This protocol included a 5-minute warm-up, 15 minutes of aerobic exercise, 15 minutes of resistance exercise, and a 5-minute cool-down. The control group received a 30-minute educational session on exercise and workplace ergonomics.

Pain sensitivity was assessed using pressure pain threshold measurements obtained with a digital algometer at the C2, C5, and upper trapezius regions. Neck pain, overall body pain perception, and fatigue were evaluated using numerical rating scales (0-10).

Sample size was calculated using G*Power (v3.1.9.6) based on a previous study (effect size = 0.165 for a three-group design), with an alpha level of 0.05 and power of 0.80, resulting in a required sample of 78 participants. Considering a 20% drop-out rate, 95 participants were targeted.

Statistical analyses were performed using SPSS. Data normality was assessed using the Shapiro-Wilk test. Baseline differences between groups were analyzed using ANOVA and chi-squared tests. The primary analysis evaluated group × time interactions using repeated-measures ANOVA (T0, T1, T2), with Bonferroni post-hoc tests applied when appropriate. Statistical significance was set at p \< 0.05.

The study focused on exercise-induced hypoalgesia (EIH) and aimed to compare the immediate and short-term responses to different exercise modalities in a working population with chronic neck pain.

02

Conditions studied

  • Neck Pain Musculoskeletal
  • Work Related Musculoskeletal Disorders

Keywords

  • Exercise-induced hypoalgesia
  • Acute effect of exercise
  • Chronic Neck Pain
  • Pressure Pain Threshold
  • Aerobic Exercise
  • Resistance Exercise
  • Ergonomic Risk
03

In context

Lead sponsor

Hacettepe University is the lead sponsor of 983 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Aged 20-65 years
  • Diagnosed with chronic non-specific neck pain within the past year
  • Neck pain intensity ≥4 on a numerical rating scale for at least 3 months
  • Actively employed for at least 1 year in similar occupational conditions
  • High ergonomic risk (Rapid Upper Limb Assessment - RULA score ≥3)

Exclusion criteria

Exclusion Criteria:

  • Neurological, cardiopulmonary, or rheumatological disorders
  • History of cervical surgery or traumatic injury
  • Specific cervical or lumbar pathology
  • Whiplash injury, or any traumatic musculoskeletal injury
  • Recent physical therapy or regular exercise in the past six months
  • Neck pain unresponsive to conservative treatment
  • Diagnosed thoracic outlet syndrome, rotator cuff pathology, vertebrobasilar insufficiency, or frozen shoulder
  • Pregnancy
  • Use of antidepressant medication
  • Positive clinical tests (Spurling, cervical distraction, Valsalva, radial, ulnar, and median nerve tension tests)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
78 participants (actual)

Study arms

  • Experimental
    Aerobic Exercise

    Participants performed moderate-intensity cycling using a recumbent ergometer in a single 40-minute session, including a 5-minute warm-up, 30 minutes of aerobic exercise, and a 5-minute cool-down.

    Behavioral: Aerobic Exercise

  • Experimental
    Combined Exercise

    Participants performed a combination of aerobic and resistance exercises in a single 40-minute session, including a 5-minute warm-up, 15 minutes of aerobic exercise, 15 minutes of resistance training targeting cervical and upper-extremity muscles, and a 5-minute cool-down.

    Behavioral: Combined Exercise

  • Active comparator
    Informed Control

    A 30-minute educational session on exercise benefits, workplace ergonomics, and postural recommendations. Participants remained seated for 5 minutes before and after the session.

    Behavioral: Informed Control

Interventions

  • BehavioralAerobic Exercise

    Moderate-intensity aerobic exercise performed using a recumbent cycle ergometer in a single 40-minute session. The protocol included a 5-minute warm-up, 30 minutes of continuous cycling, and a 5-minute cool-down. Exercise intensity was maintained at 64-76% of maximum heart rate and adjusted individually throughout the session. No resistance or strength training exercises were included.

  • BehavioralCombined Exercise

    Participants performed a combination of aerobic and resistance exercises in a single 40-minute session. The protocol included a 5-minute warm-up, 15 minutes of moderate-intensity aerobic exercise (64-76% HRmax, Borg RPE 11-14), 15 minutes of resistance exercises targeting cervical and upper-extremity muscles, and a 5-minute cool-down. The resistance program focused on cervical motor control and scapular stabilization, including chin tuck, cervical retraction with extension, scapular retraction, vertical pulling, horizontal shoulder abduction, scapular plane abduction, and shoulder elevation. Each exercise was performed for 8-10 repetitions in two sets with 30-second rest intervals. All exercises were supervised and performed with proper postural alignment.

  • BehavioralInformed Control

    Participants attended a 30-minute educational session on exercise benefits, workplace ergonomics, and postural recommendations. Participants remained seated for 5 minutes before and after the session.

06

What researchers measure

Primary outcomes

  1. Pressure Pain Threshold

    Pressure pain threshold is assessed using a digital algometer to evaluate pain sensitivity. The value at which the sensation of pressure first becomes painful is recorded in lbf/cm². Three consecutive measurements are obtained at each site, and the mean value is used for analysis. Measurements are obtained bilaterally at the C2 region, C5 region, and upper trapezius muscle.

    Time frame: Three time points: before the intervention (T0), immediately after the intervention (T1), and 20 minutes after the intervention (T2).

Secondary outcomes

  1. Acute Neck Pain Perception

    Acute neck pain intensity is assessed using a numerical rating scale (0-10), a simple and widely used tool for evaluating pain. Participants are asked to select the number that best represents their pain intensity. Zero indicates no pain, and 10 represents the worst imaginable pain.

    Time frame: Assessments are performed at three time points: before the intervention (T0), immediately after the intervention (T1), and 20 minutes after the intervention (T2).

  2. Acute Overall Body Pain Perception

    Acute overall body pain perception is assessed using a numerical rating scale (0-10), a simple and widely used tool for evaluating pain. Participants are asked to select the number that best represents their pain intensity. Zero indicates no pain, and 10 represents the worst imaginable pain.

    Time frame: Assessments are performed at three time points: before the intervention (T0), immediately after the intervention (T1), and 20 minutes after the intervention (T2).

  3. Acute Fatigue

    Acute fatigue is assessed using a numerical rating scale (0-10), a simple and widely used tool for evaluating fatigue. Participants are asked to select the number that best represents their fatigue intensity. Zero indicates no fatigue, and 10 represents the worst imaginable fatigue.

    Time frame: Assessments are performed at three time points: before the intervention (T0), immediately after the intervention (T1), and 20 minutes after the intervention (T2).

Other outcomes

  1. Ergonomic Risk Level - Rapid Upper Limb Assessment (RULA)

    Ergonomic risk level is assessed using the RULA method to classify participants' workplace-related ergonomic risk at baseline.

    Time frame: Baseline

  2. Functional Aerobic Capacity 6-Minute Walk Test (6MWT)

    Functional aerobic capacity is assessed using the 6MWT. The total walking distance is recorded to ensure that participants have sufficient functional capacity to safely complete the study procedure.

    Time frame: Baseline

  3. Physical Activity Level (IPAQ-SF)

    Physical activity level is assessed using the International Physical Activity Questionnaire Short Form (IPAQ-SF). The questionnaire evaluates the time spent in walking, moderate, and vigorous physical activities over the past 7 days. Time Frame: Baseline

    Time frame: Baseline

07

Study locations

1 site
  • Faculty of Physical Therapy adn Rehabilitation, Hacettepe University
    Ankara, Çankaya 06100, Turkey (Türkiye)
08

References and documents

Publications

  • Rice D, Nijs J, Kosek E, Wideman T, Hasenbring MI, Koltyn K, Graven-Nielsen T, Polli A. Exercise-Induced Hypoalgesia in Pain-Free and Chronic Pain Populations: State of the Art and Future Directions. J Pain. 2019 Nov;20(11):1249-1266. doi: 10.1016/j.jpain.2019.03.005. Epub 2019 Mar 21. PubMed 30904519 ↗
  • Senarath ID, Chen KK, Weerasekara I, de Zoete RMJ. Exercise-induced hypoalgesic effects of different types of physical exercise in individuals with neck pain: A systematic review and meta-analysis. Pain Pract. 2023 Jan;23(1):110-122. doi: 10.1111/papr.13150. Epub 2022 Aug 2. PubMed 35869789 ↗
  • Anarte-Lazo E, Bernal-Utrera C, Lopez-Amor M, Porras-Valencia E, Ruy-Diaz-Rojas FJ, Falla D, Rodriguez-Blanco C. Exercise-induced hypoalgesia after aerobic versus neck-specific exercise in people with acute/subacute whiplash-associated disorders: protocol for a randomised controlled trial. BMJ Open. 2022 Sep 22;12(9):e061679. doi: 10.1136/bmjopen-2022-061679. PubMed 36137629 ↗
  • Acikalin E, Atasavun Uysal S. Acute effects of aerobic versus combined aerobic and cervical-upper extremity resistance exercise on pressure pain threshold, pain perception, and fatigue in workers exposed to high ergonomic risk with chronic non-specific neck pain: a randomized controlled trial. BMC Musculoskelet Disord. 2026 Jul 14. doi: 10.1186/s12891-026-10182-8. Online ahead of print. PubMed 42449286 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07546838
Lead sponsor
Hacettepe University
Collaborators
The Scientific and Technological Research Council of Turkey
Responsible party
Eda ACIKALIN (Physiotherapist, PhD Candidate, Hacettepe University) — Principal investigator
First posted
Apr 23, 2026
Start date
May 22, 2025
Primary completion
Oct 1, 2025
Completion
Oct 30, 2025
Last update
Apr 23, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion