Association Between Sleep Disorders, Neck Pain, and Depression

NCT ID: NCT07032480

Last Updated: 2025-07-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

265 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-26

Study Completion Date

2026-06-22

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This cross-sectional observational study investigates the association between sleep quality, neck pain-related disability, and depression symptoms in young adults aged 18-28. The research reveals that poor sleep quality is significantly associated with higher depression scores and increased neck disability, emphasizing the need for integrative approaches targeting sleep quality to improve mental and musculoskeletal health outcomes.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Health Risk Behaviors

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Healthy Sleep Group

Participants who scored 0-5 on the Pittsburgh Sleep Quality Index (PSQI), indicating good sleep quality.

Survey-Based Assessment

Intervention Type BEHAVIORAL

Participants completed standardized questionnaires including the Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), and Neck Disability Index (NDI) to evaluate psychological and functional outcomes associated with sleep quality. No experimental intervention was administered.

Poor Sleep Group

Participants who scored between 6-10 on the PSQI, indicating impaired sleep quality.

Survey-Based Assessment

Intervention Type BEHAVIORAL

Participants completed standardized questionnaires including the Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), and Neck Disability Index (NDI) to evaluate psychological and functional outcomes associated with sleep quality. No experimental intervention was administered.

Chronic Sleep Disorder Group

Participants who scored above 10 on the PSQI, indicating persistent and clinically relevant sleep disturbances.

Survey-Based Assessment

Intervention Type BEHAVIORAL

Participants completed standardized questionnaires including the Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), and Neck Disability Index (NDI) to evaluate psychological and functional outcomes associated with sleep quality. No experimental intervention was administered.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Survey-Based Assessment

Participants completed standardized questionnaires including the Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), and Neck Disability Index (NDI) to evaluate psychological and functional outcomes associated with sleep quality. No experimental intervention was administered.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Aged 18-28
* No history of physical or psychological illness
* Able to provide informed consent
* Voluntarily agreed to participate

Exclusion Criteria

* History of chronic illness or psychiatric disorder
* Communication difficulties
Minimum Eligible Age

18 Years

Maximum Eligible Age

28 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Saglik Bilimleri Universitesi

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

ESRA PEHLIVAN

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Saglik Bilimleri Universitesi

Istanbul, Üsküdar, Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Esra Pehlivan

Role: CONTACT

Ayşegül Demirel

Role: CONTACT

+90 539 308 99 38

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Esra Pehlivan, Associate Professor

Role: primary

02164189616

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Sleep&Neck&Depression

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Sleep Health, Inflammation, and Emotion Study
NCT02270619 COMPLETED EARLY_PHASE1
Impact of Orthopedic Surgery on Workers' Sleep
NCT06854913 ENROLLING_BY_INVITATION NA