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临床试验/NCT07167888
NCT07167888尚未招募不适用

The Prevalence of Neck and Low Back Pain With a Randomised Controlled Trial Comparing Spine-Specific and Non-Spine Specific Exercise Interventions in Nursing Students at The University of the West Indies, Mona: A Two-Phase Study

The University of The West Indies1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2026年4月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
400
试验地点
1
主要终点
Change from Baseline in the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ)

研究概览

简要总结

The purpose of this study is to identify the prevalence of neck and low back pain in nursing students enrolled at the University of the West Indies, Mona; to assess their knowledge, attitude and practice of good spine health and to determine the outcome of a standardised spine exercise program on nursing students experiencing neck and low back pain, using a prospective randomised control design.

详细描述

Neck and low back pain are among the most common musculoskeletal conditions worldwide. Although often self-limiting, these conditions can become disabling, negatively affecting productivity, social participation, and activities of daily living. Occupational factors, prolonged sitting, sustained computer use, awkward postures, and repetitive neck movements are recognised contributors to spinal pain. Nursing students are particularly vulnerable to musculoskeletal disorders, with risk beginning during their training years. During the preclinical phase, students spend prolonged periods attending lectures, studying, and completing assignments, often involving sustained sitting and computer use. In the clinical phase, students are exposed to physically demanding tasks such as prolonged standing, ward rounds, assisting with procedures, and manual patient handling, including lifting and repositioning patients. These activities, combined with poor ergonomic practices and reduced core stability, may contribute to the development of neck and low back pain. International studies have reported a high prevalence of musculoskeletal pain among nursing and medical students, particularly during clinical training. Factors such as increased computer use, elevated body mass index, prior trauma, and family history of musculoskeletal disorders have been identified as contributing risk factors. However, no published study has investigated the prevalence of neck and low back pain among nursing students in Jamaica or the wider Caribbean. Exercise therapy is widely recognised as an effective non-pharmacologic intervention for both acute and chronic low back pain, with evidence showing improvements in pain reduction and functional outcomes. Exercise enhances muscular strength, flexibility, and spinal stability, while promoting nutrient exchange within spinal structures, supporting overall spinal health and reducing the risk of injury. This study aims to determine the prevalence of neck and low back pain among nursing students at The University of the West Indies, Mona, and to compare the effectiveness of a standardized spine-specific exercise programme versus non-spine-specific exercises in reducing pain and improving knowledge, attitudes, and practices related to spinal health. It will be conducted in two phases and guided by a descriptive and experimental framework. In the first phase, the descriptive phase, a cross-sectional design will be used to assess the prevalence of neck and low back pain (NLBP) among all year groups of nursing students at The University of the West Indies, Mona. The University of the West Indies, Mona, currently enrolls approximately 400 nursing students across four years of training. Participants will complete questionnaires to determine the presence of musculoskeletal discomfort in the neck and low back pain, as well as their knowledge, attitude, and practice related to spine health. In the second phase, the experimental phase, nursing students who report musculoskeletal discomfort will be randomised into intervention and control groups. The intervention group will participate in an eight-week spine-specific exercise program, while the control group will receive a non-spine specific exercise in parallel during the study period. Pre- and post-intervention data will be collected using the Numeric Rating Scale (NRS), the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), and custom questionnaires (Questionnaires A & B) to assess changes in assessing knowledge, attitudes and practices toward musculoskeletal health, changes in perceived pain and participants' functional status.

Participant confidentiality will be strictly maintained, with each participant assigned a study identification number. Demographic data, presenting complaints, and outcome measures will be collected for study purposes and managed securely using REDCap, a password-protected, web-based platform compliant with national data protection standards. Statistical analysis will be conducted using the International Business Machines Corporation Statistical Product and Service Solutions (IBM SPSS software), and all study records will be securely stored and destroyed three years after study completion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • All students enrolled in the student nursing program at the University of the West Indies, Mona Campus, Jamaica during the period October 4, 2025 to October 3,
  • Individuals who express a willingness to consent to the study.
  • Individuals who express a willingness to adhere to the standardised exercise program for the stipulated period.

排除标准

  • Individuals with a history of having spine surgery.
  • Individuals who were previously diagnosed with spine pathology and currently receiving rehabilitation therapy.
  • Individuals who express an unwillingness to participate in the study.

研究组 & 干预措施

Clinical Control (Group A)

Experimental

All participants will complete the Cornell Musculoskeletal Discomfort Questionnaires (CMDQ) to assess the frequency, discomfort and interference with work due to musculoskeletal pain; the Numeric Rating Scale (NRS) to assess for perceived pain; as well as Questionnaire A to assess their knowledge, attitude and practice towards musculoskeletal problems of neck or low back pain. Participants who are found to have neck or low back pain will be randomised into two (2) groups: a clinical control group (Group A) and an intervention group (Group B). Group A will be given a non-spine specific exercise program over an eight (8) week period after which time, participants will be reassessed using the CMDQ and NRS, as well as a Questionnaire B to evaluate for changes in their knowledge, attitude and practice towards musculoskeletal problems of the neck and low back pain.

干预措施: Clinical Control Group (Group A) (Behavioral)

Spine Exercise Program (Group B)

Experimental

All participants will complete the Cornell Musculoskeletal Discomfort Questionnaires (CMDQ) to assess the frequency, discomfort and interference with work due to musculoskeletal pain; the Numeric Rating Scale (NRS) to assess for perceived pain; as well as Questionnaire A to assess their knowledge, attitude and practice towards musculoskeletal problems of neck or low back pain. Participants who are found to have neck or low back pain will be randomised into two (2) groups: a clinical control group (Group A) and an intervention group (Group B). Group B will be given a standardised spine-specific exercise program over an eight (8) week period, after which time they will be be reassessed using the CMDQ and NRS, as well as Questionnaire B to evaluate for changes in their knowledge, attitude and practice towards musculoskeletal problems of the neck and low back pain, having received the intervention.

干预措施: Spine Exercise Program (Group B) (Behavioral)

结局指标

主要结局

Change from Baseline in the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ)

时间窗: From enrollment to the end of treatment at eight (8) weeks

The Cornell Musculoskeletal Discomfort Questionnaire measures the frequency, discomfort and interference with work due to musculoskeletal pain, as reported by participants. The individually reported frequency score is then multiplied by the discomfort score and by the interference score to determine overall severity of pain experienced. This tallied score is then classified by severity into: no discomfort (0), mild (1 to 4.5), moderate (5 to 14), severe (15 - 45) and very severe (45 or higher). All participants will complete this assessment upon enrollment, as well as after an eight (8) week period of treatment, to evaluate any changes in their reported scores.

次要结局

  • Change from Baseline in the Numeric Rating Scale (NRS)(From Enrollment to the end of treatment at 8 weeks)
  • Knowledge, Attitude and Practice towards Musculoskeletal Problems of Neck and Low back Pain (Questionnaire A)(Done at the time of enrollment (Baseline))
  • Change from Baseline in Knowledge, Attitude and Practice Towards Musculoskeletal Problems of Neck and Low Back Pain (Questionnaire B)(From Enrollment to the end of treatment at 8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paula Dawson, MBBS

Head, Physical Medicine and Rehabilitation. Principal Investigator

The University of The West Indies

研究点 (1)

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