ClinicalTrials.gg
CompletedNCT07872267Updated Oct 13, 2026

Neck and Shoulder Pain in Homemakers

An observational study in Neck Pain, Shoulder Pain and Musculoskeletal Pain, sponsored by Lokman Hekim University. Completed at 1 site in Turkey (Türkiye). Open to female participants. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Lokman Hekim University · Observational

Updated Oct 13, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
100
Sex
Female
01

Study summary

This cross-sectional observational study aims to investigate the prevalence and associated factors of neck and shoulder pain in homemakers aged 25-55 years. The study will examine the relationships between neck and shoulder pain and demographic characteristics, duration and type of housework, fatigue, physical activity, smartphone and social media use, hobbies, posture, functional status, instrumental activities of daily living, and health-related quality of life. Neck-related disability will be assessed using the Neck Disability Index, upper extremity function using the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire, instrumental activities of daily living using the Lawton and Brody Instrumental Activities of Daily Living Scale, quality of life using the SF-12 Health Survey, and posture using the New York Posture Rating Chart. The findings are expected to contribute to identifying factors associated with neck and shoulder pain in homemakers and to inform future preventive and rehabilitative approaches.

Read the detailed description

This cross-sectional observational study is designed to investigate neck and shoulder pain and the factors associated with these complaints in homemakers aged 25-55 years. Homemakers are frequently exposed to repetitive upper extremity activities, prolonged postures, domestic workload, smartphone use, and other daily activities that may contribute to musculoskeletal symptoms. The study therefore aims to evaluate neck and shoulder pain within a multidimensional framework including demographic, lifestyle, physical, functional, and health-related characteristics.

Participants will be homemakers who have been actively engaged in housework for at least five years and who provide written informed consent. Women with orthopedic, neurological, or rheumatological diseases, thoracic outlet syndrome, cervical radiculopathy, diagnosed cervical disc herniation, recent surgery or injury affecting the neck or shoulder region, pregnancy or postpartum status, recent initiation of medication that may affect neck or shoulder pain, or acute trauma-related neck or shoulder pain will be excluded.

Demographic and lifestyle characteristics, including age, body weight, height, body mass index, marital status, duration of being a homemaker, number of children, menopausal status, smoking and alcohol use, daily duration and type of housework, fatigue severity, hobbies, smartphone use, social media use, and average daily step count, will be recorded using a general assessment form.

Neck and shoulder pain will be evaluated separately in terms of frequency, duration, and pain severity during the daytime, nighttime, movement, and rest. Neck-related disability will be assessed using the Neck Disability Index, while upper extremity functional status will be evaluated using the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire. Instrumental activities of daily living will be assessed using the Lawton and Brody Instrumental Activities of Daily Living Scale, health-related quality of life using the SF-12 Health Survey, and posture using the New York Posture Rating Chart.

All assessments will be performed face-to-face. The study includes no therapeutic intervention or medical treatment. Data will be analyzed to examine the prevalence of neck and shoulder pain and the relationships between pain, functional status, posture, daily activities, lifestyle characteristics, and quality of life.

02

Conditions studied

  • Neck Pain
  • Shoulder Pain
  • Musculoskeletal Pain

Keywords

  • Homemakers
  • Fatigue
  • Posture
  • Physical activity
  • Housework
  • Activities of daily living
  • Quality of life
03

In context

Neck Pain

1,259 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's enrollment of 100 is close to the median of 93 across 218 observational studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Lokman Hekim University is the lead sponsor of 42 studies on the registry; 16 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will consist of homemakers aged 25-55 years living in Ankara, Türkiye, who have been actively engaged in housework for at least five years and meet the study eligibility criteria. Participants will be recruited on a voluntary basis from the community.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female homemakers aged 25-55 years
  • Actively engaged in housework for at least 5 years
  • Willing to participate in the study and able to provide written informed consent

Exclusion criteria

Exclusion Criteria:

  • Presence of any orthopedic, neurological, or rheumatological disease (e.g., fracture, stroke, osteoporosis)
  • Thoracic outlet syndrome, cervical radiculopathy, or diagnosed cervical disc herniation
  • Surgery or injury affecting the neck or shoulder region within the previous 6 months
  • Pregnancy or postpartum period
  • Initiation of any medication that may affect neck or shoulder pain within the previous 6 months
  • Neck or shoulder pain resulting from acute trauma
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • Homemakers

    Women aged 25-55 years who have been actively engaged in housework for at least five years and meet the study eligibility criteria will be included in this observational cohort. Participants will undergo assessments of neck and shoulder pain, fatigue, daily activities, physical activity, smartphone use, posture, functional status, instrumental activities of daily living, and health-related quality of life. No intervention or treatment will be administered as part of the study.

    Other: Observational Assessment

Interventions

  • OtherObservational Assessment

    Participants will undergo a one-time, face-to-face observational assessment including evaluation of neck and shoulder pain, fatigue, daily activities, physical activity, smartphone use, posture, functional status, instrumental activities of daily living, and health-related quality of life. No therapeutic intervention or medical treatment will be administered as part of the study.

06

What researchers measure

Primary outcomes

  1. Prevalence of Neck Pain

    Presence of neck pain will be recorded as yes/no based on participant self-report.

    Time frame: Baseline

  2. Prevalence of Shoulder Pain

    Presence of shoulder pain will be recorded as yes/no based on participant self-report.

    Time frame: Baseline

Secondary outcomes

  1. Neck-Related Disability

    The Neck Disability Index consists of 10 items scored from 0 to 5. Total scores range from 0 to 50, with higher scores indicating greater neck-related disability.

    Time frame: baseline

  2. Upper Extremity Disability

    The Disabilities of the Arm, Shoulder and Hand Questionnaire evaluates symptoms and difficulty performing upper extremity activities. Scores range from 0 to 100, with higher scores indicating greater upper extremity disability.

    Time frame: baseline

  3. Instrumental Activities of Daily Living

    The Lawton and Brody Instrumental Activities of Daily Living Scale evaluates independence in eight instrumental activities of daily living. Total scores range from 0 to 8, with higher scores indicating greater independence.

    Time frame: baseline

  4. Health-Related Quality of Life

    Health-related quality of life will be assessed using the 12-item Short Form-12, covering physical and mental health-related domains. Higher scores indicate better health status and quality of life.

    Time frame: baseline

  5. Postural Alignment

    Posture will be assessed across 13 body regions by New York Posture Rating Chart. Total scores range from 13 to 65, with higher scores indicating better postural alignment.

    Time frame: baseline

07

Study locations

1 site
  • Lokman Hekim University, Ankara, Ankara
    Ankara, Ankara 06370, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07872267
Lead sponsor
Lokman Hekim University
Responsible party
Demet Öztürk (Assist. Prof., Lokman Hekim University) — Principal investigator
First posted
Oct 13, 2026
Start date
Feb 1, 2026
Primary completion
Aug 1, 2026
Completion
Sep 20, 2026
Last update
Oct 13, 2026

Oversight

Data monitoring committee
No
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 Oct 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