Mindfulness Plus Supervised Rehabilitation vs Supervised Rehabilitation Alone for Chronic Neck Pain in Office Workers
Effect of Mindfulness Combined With Supervised Rehabilitation Versus Supervised Rehabilitation Alone in Office Workers With Chronic Neck Pain: Protocol for a Randomized Controlled Trial
The goal of this clinical trial is to learn if adding mindfulness to supervised rehabilitation exercises improves outcomes in office workers with chronic neck pain. It will also evaluate the impact of this combined approach on psychosocial factors and quality of life. The main questions it aims to answer are:
Does mindfulness combined with supervised exercises reduce neck pain intensity more than supervised exercises alone? Does the combined intervention improve neck-related disability, psychosocial outcomes, and quality of life?
Researchers will compare a mindfulness-based intervention plus supervised rehabilitation exercises to supervised rehabilitation exercises alone to determine whether the combined approach provides additional benefit.
Participants will:
Be randomly assigned to receive either mindfulness plus supervised exercises or supervised exercises alone for 8 weeks Attend weekly 60-minute mindfulness sessions (experimental group only) and twice-weekly supervised exercise sessions Undergo assessments at the beginning and at the end of the intervention period
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Amr Chaabeni, MD
- 電話番号:+21626729316
- メール:amrch97@gmail.com
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Office workers aged 18 years or older
- diagnosed with chronic neck pain for more the three months
Exclusion Criteria:
- history of neck surgery
- history of cervical trauma
- history of neurological disorders affecting the neck or upper extremities
- currently receiving other treatments for neck pain, such as injections or surgical interventions
- Participants with significant psychiatric disorders that could interfere with study participation or adherence to the intervention
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Mindfulness arm
Participants in the intervention group will follow an 8-week supervised program combining mindfulness training and therapeutic exercise.
The intervention includes one weekly 60-minute mindfulness session and two supervised exercise sessions (each lasting 30 minutes), delivered by a trained professional according to a standardized protocol.
Mindfulness sessions will be conducted in small groups and incorporate structured practices including mindful breathing, body scanning, guided imagery, and relaxation techniques.
Mindful breathing focuses on sustained, non-judgmental attention to the breath to enhance present-moment awareness and modulate pain perception.
Body scanning involves systematic attention to body regions to increase awareness of sensations and tension.
Guided imagery and relaxation techniques (e.g., progressive muscle relaxation, meditation) aim to promote relaxation and reduce pain-related distress
|
Mindfulness training incorporates structured practices such as mindful breathing, body scanning, guided imagery, and relaxation techniques.
Mindful breathing focuses on sustained, non-judgmental attention to the breath to enhance present-moment awareness and modulate pain perception.
Body scanning involves systematic attention to body regions to increase awareness of physical sensations and tension.
Guided imagery and relaxation techniques, including progressive muscle relaxation and meditation, aim to promote relaxation and reduce pain-related distress.
他の名前:
The program will focus on standardized stretching, strengthening, and postural exercises commonly prescribed in routine musculoskeletal rehabilitation. Stretching exercises will target the cervical region and will include neck flexion, extension, and lateral flexion stretches, each performed in a seated upright position, held for 30 seconds, and repeated three times per direction. Strengthening exercises will emphasize cervical muscle activation and endurance and will include neck retraction exercises (chin pull-back) and isometric neck strengthening performed against manual resistance in flexion, extension, and lateral directions, with standardized hold times and repetitions. Postural exercises will focus on cervical and scapular alignment and will include chin tucks and shoulder blade squeezes, performed with controlled holds and repeated sets.
他の名前:
|
|
アクティブコンパレータ:Control arm
Participants in the control group will follow an 8-week supervised conventional exercise program consisting of two sessions per week, each lasting 30 minutes, delivered according to a standardized protocol.
The program includes stretching, strengthening, and postural exercises commonly used in musculoskeletal rehabilitation.
Stretching targets the cervical region (flexion, extension, lateral flexion), with each stretch held for 30 seconds and repeated three times.
Strengthening focuses on cervical muscle activation and endurance through neck retraction and isometric exercises against manual resistance in multiple directions.
Postural exercises emphasize cervical and scapular alignment, including chin tucks and scapular retraction performed with controlled holds.
All sessions are supervised, and participants continue their usual occupational activities.
|
The program will focus on standardized stretching, strengthening, and postural exercises commonly prescribed in routine musculoskeletal rehabilitation. Stretching exercises will target the cervical region and will include neck flexion, extension, and lateral flexion stretches, each performed in a seated upright position, held for 30 seconds, and repeated three times per direction. Strengthening exercises will emphasize cervical muscle activation and endurance and will include neck retraction exercises (chin pull-back) and isometric neck strengthening performed against manual resistance in flexion, extension, and lateral directions, with standardized hold times and repetitions. Postural exercises will focus on cervical and scapular alignment and will include chin tucks and shoulder blade squeezes, performed with controlled holds and repeated sets.
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Neck pain using the VAS
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
Neck pain intensity is the primary outcome, assessed using the Visual Analogue Scale (VAS).
Participants rate their pain on a 100-mm horizontal line ranging from "no pain" (0) to "worst imaginable pain" (100), with higher scores indicating greater pain intensity.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Neck Disability Index (NDI)
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The NDI consists of 10 items (pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation), each scored from 0 to 5, yielding a total score between 0 and 50.
Higher scores indicate greater disability.
the NDI have a strong internal consistency, high test-retest reliability, and sensitivity to clinical change.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Fear of movement using the Tampa Scale for Kinesiophobia
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The Tampa Scale for Kinesiophobia (TSK) will be employed to evaluate participants' fear of movement and re-injury.
The scale consists of 17 items, each rated from 1 to 4, with higher scores indicating greater kinesiophobia.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Pain catastrophizing
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
Catastrophic thinking will be assessed with the Pain Catastrophizing Scale (PCS).
This instrument evaluates the extent to which individuals engage in catastrophic thoughts related to their pain.
it consists of 13 items, each ranging from 0 (not at all) to 4 (all the time).
Higher scores indicate greater levels of catastrophizing.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Perceived stress
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The Perceived Stress Scale (PSS) evaluates the perception of stress in individuals and is essential for understanding how mindfulness interventions may reduce stress levels among participants.
the PSS measures perceived stress over the past month.
it includes 10 items each rated from 0 (never) to 4 (very often).
Higher scores indicate greater perceived stress.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Anxiety and depression symptoms using the Hospital Anxiety and Depression Scale (HADs)
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The HADS is a validated instrument widely used in both hospital and general populations to evaluate psychological distress, which is particularly relevant in the context of chronic pain.
It consists of 14 items divided into two subscales, anxiety and depression, with 7 items each from 0 to 3. higher subscale scores reflect more severe symptoms of anxiety or depression.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Sleep quality using the Pittsburgh Sleep Quality Index (PSQI)
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The PSQI is a validated self-report instrument that evaluates sleep quality and disturbances over the past month.
It comprises 19 items with a score ranging from 0 to 21, with higher scores indicating poorer sleep quality.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
|
Health-related quality of life using the SF-12
時間枠:at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
The SF-12 evaluates overall well-being by capturing both physical and mental health dimensions.
It provides two standardized summary scores: the Physical Component Score (PCS) and the Mental Component Score (MCS), each range from 0 to 100, with higher scores indicating better health status.
|
at participant enrollment (baseline) and ending immediately after the 8-week intervention
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- MINDEX-NECK-RCT-2026
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。