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临床试验/NCT05851586
NCT05851586已完成不适用

Effectiveness of Physical Therapy Intervention in Pre-Clinical Dental Students

Joshua Subialka1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2023年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
16
试验地点
1
主要终点
Pain Intensity

研究概览

简要总结

The main purpose of our study is to assess whether guided strength training and stretching intervention with a written home exercise program is more effective than a home exercise program alone for pre-clinical dental students in improving and preventing pain associated with dental laboratory practice. Secondary aims will be to assess relationships between strength and quality of life measures of an individual and pain levels.

详细描述

Musculoskeletal (MSK) pain has been identified as a major concern among dental professionals. This can lead to decreased productivity, efficiency and quality of work along with higher costs for the medical system. The body region that is affected the most is the neck, followed by the back and shoulders.

Ergonomic assessments and interventions can identify the areas of concern with workplace set up, however, training the muscles to adapt to abnormal postures may be an effective way of increasing the resilience of the MSK system while decreasing MSK pain as well. Specifically, strength training and stretching has been well researched as a way to prevent and improve pain for neck pain, low back pain and shoulder pain. Physical therapists are well trained in prevention and treatment of injuries, including a wealth of knowledge regarding strength training and stretching for specific regions. The main purpose of our study is to assess whether guided strength

Thus, the main purpose of our study is to assess whether guided strength training and stretching intervention with a written home exercise program is more effective than a home exercise program alone for pre-clinical dental students in improving and preventing pain associated with dental laboratory practice. The secondary aim will be to assess the relationships between strength and quality of life measures of an individual and pain levels.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults ages 18+
  • Current 2nd year university dental students

排除标准

  • Any type of musculoskeletal surgery in the past 6 months

研究组 & 干预措施

Supervised exercise + home exercise program

Experimental

The intervention group (supervised exercise) which will receive supervised strengthening and stretching exercises by a licensed physical therapist in a group setting 2 times per month for 30 minutes each session as well as a home exercise program with general stretching and strengthening exercises for various body parts (focusing on neck, thoracic spine, lumbar spine, shoulder and hand/wrist) that will be identical to the home exercise program only group.

干预措施: Supervised exercise + home exercise program (Procedure)

Home exercise program only

Active Comparator

The home exercise program only group will be provided with a written home exercise program consisting of general stretching and strengthening exercises for various body parts (focusing on neck, thoracic spine, lumbar spine, shoulder and hand/wrist). The exercise programs will be identical for both the supervised exericse and the home exercise program only groups.

干预措施: Home exercise program only (Procedure)

结局指标

主要结局

Pain Intensity

时间窗: 11 months

Visual analog scale (0-10 rating)

Patient-Reported Outcomes Measurement Information System (PROMIS)

时间窗: 11 months

PROMIS® is a publicly available system of highly reliable, precise measures of patient-reported health status for physical, mental, and social well-being. This will be measured via electronic survey.

Patient-Reported Outcomes Measurement Information System (PROMIS)

时间窗: Baseline

PROMIS® is a publicly available system of highly reliable, precise measures of patient-reported health status for physical, mental, and social well-being. This will be measured via electronic survey.

Patient-Reported Outcomes Measurement Information System (PROMIS)

时间窗: Intervention conclusion (7 months)

PROMIS® is a publicly available system of highly reliable, precise measures of patient-reported health status for physical, mental, and social well-being. This will be measured via electronic survey.

Pain Intensity

时间窗: Baseline

Visual analog scale (0-10 rating)

Pain Intensity

时间窗: Intervention conclusion (7 months)

Visual analog scale (0-10 rating)

次要结局

  • Lower Trapezius Manual Muscle Test(11 months)
  • Middle Trapezius Manual Muscle Test(11 months)
  • Pec Minor Length Test(11 months)
  • Cervical Flexor Endurance Test(11 months)
  • Pec Minor Length Test(Baseline, intervention conclusion (7 months), and 4 month follow up prior to beginning clinical rotations.)
  • Pec Minor Length Test(Intervention conclusion (7 months))
  • Middle Trapezius Manual Muscle Test(Baseline)
  • Middle Trapezius Manual Muscle Test(Intervention conclusion (7 months))
  • Lower Trapezius Manual Muscle Test(Baseline)
  • Lower Trapezius Manual Muscle Test(Intervention conclusion (7 months))
  • Cervical Flexor Endurance Test(Baseline)
  • Cervical Flexor Endurance Test(Intervention conclusion (7 months))

研究者

发起方
Joshua Subialka
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Joshua Subialka

Assistant Professor, Associate Investigator

Midwestern University

研究点 (1)

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