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临床试验/NCT06671665
NCT06671665招募中不适用

Effect of Manual Therapy on Low Back Pain in Osteopenic Postmenopausal Women

Cairo University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年11月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Assessment of Low back pain severity

研究概览

简要总结

The purpose of this study is to determine the effect of manual therapy on low back pain in osteopenic postmenopausal women.

详细描述

Women spend nearly one-third of their life in menopause. In this period, besides other comorbid conditions, women suffer from various musculoskeletal disorders also. One such problem is chronic low back pain which is more prevalent in post-menopausal women. This condition affects daily living activities of a person ranging from standing up, walking, bending over, lifting, traveling, social interaction, dressing to sleeping, living with ongoing pain causes depression, anxiety, deterioration in quality of life for women themselves. Despite this, little attention has been paid to pain in the spine/low back ache which are equally prevalent in this period of life.

Although this poses a great medical and socioeconomic challenge to such extent that some researchers call it a lifestyle disease. It is the main cause of absence in the workplace and the 2nd cause of visiting primary health-care professionals. Spine pain has negative psychological consequences as it impairs daily functioning. Therefore, finding an effective method for treatment is important.

Manual treatments are one of the most applied methods within physiotherapy approaches in recent years. Manual treatment (in the form of craniosacral and visceral manipulation) claiming to release the tension of the muscles, ligaments, and fascia in the sacral area and activate central pain inhibitory centers. For this reason, we are conducting the present study with a new view to identify the effects of manual therapy practices in the form of craniosacral and visceral manipulation on pain, function, and BMD of the lumbar region, as well as quality of life in osteopenic post-menopausal women suffering from low back pain.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
50 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Ambulatory, sedentary, non-smoking women having natural menopause at least 1 year before participation in the study.
  • Their ages will range from 50 to 60 years old.
  • Their BMI will be > 30 kg/m
  • Pain before costal margin and above inferior gluteal fold.
  • Osteopenia.

排除标准

  • Osteoporosis.
  • Having osteoporotic fractures.
  • Having a lumbar surgery previously.
  • Neurological disorder.
  • Known diseases affecting bone quality (hyperthyroidism, hyperparathyroidism, hypercortisolism, etc).
  • Receiving any medical or hormonal therapies that could affect the bone metabolism.
  • Receiving previous manual treatment.

研究组 & 干预措施

calcium supplementation

Active Comparator

It will consist of 20 postmenopausal women. They will receive calcium supplementation daily for 12 weeks.

干预措施: calcium supplementation (Drug)

calcium supplementation + manual therapy

Experimental

It will consist of 20 postmenopausal women. They will receive the same calcium supplementation daily in addition to manual therapy (in form of craniosacral technique & general visceral mobilization) for 12 weeks.

干预措施: calcium supplementation (Drug)

calcium supplementation + manual therapy

Experimental

It will consist of 20 postmenopausal women. They will receive the same calcium supplementation daily in addition to manual therapy (in form of craniosacral technique & general visceral mobilization) for 12 weeks.

干预措施: Manual therapy (Other)

结局指标

主要结局

Assessment of Low back pain severity

时间窗: 12 weeks

Pain will be assessed by Visual analog scale (VAS). It is a scale that allows continuous data analysis and uses a 10cm line with 0 (0 = no pain) written at one end and 10 (10 = worst pain) on the other end. Subjects will be asked to place a mark along the line to denote their level of pain.

Measurement of lumbar curvature angle.

时间窗: 12 weeks

It will be measured, before and after treatment program, using a flexible ruler. The flexible ruler will be molded to the midline contour of the lumber spine from the spinous process of T12 to S2 to measure the degree of lordosis which carefully traced onto paper using pencil. Then, the lumbar curvature angle will be measured by the equation (theta angle = 4Arctang 2H/L). In this equation, the theta angle represents the magnitude of the lordotic curve, L is a straight line from the first vertebrae to the last vertebrae and the H letter is the distance between the deep point of L line and the lumbar curve.

Assessment of Lumbar Flexion

时间窗: 12 weeks

The examiner will stand behind the standing patient to identify the posterior superior iliac spines with thumbs, and then an ink mark will be drawn along the midline of the lumbar spine horizontal to the posterior superior iliac spines. Another ink mark will be made 15 cm above the original mark. The tape measure will be lined up between skin markings. With the tape pressed firmly against the subject's skin and while holding it with fingertips, the distance between superior and inferior skin marks will be measured. Then, the examiner will instruct the patient to bend forward into full lumbar flexion and the new distance between superior and inferior skin marks will be measured. The change in the difference between marks will be used to indicate the amount of lumbar flexion.

Assessment of Lumbar Extension

时间窗: 12 weeks

The examiner will follow the same procedure done previously in lumbar flexion except with the instruction. As the examiner will instruct the patient to bend backward into full extension and the new distance between superior and inferior skin marks will be measured as a straight line. The change in the difference between marks will be used to indicate the amount of lumbar extension.

Assessment of Lumbar Lateral bending to the right side

时间窗: 12 weeks

Measuring the distance between the tip of the middle finger and the floor when the patient stands upright, heels, buttocks and shoulders against the wall, and bends sideways without lifting the opposite foot off the ground.

Assessment of Lumbar Lateral bending to the left side

时间窗: 12 weeks

Measuring the distance between the tip of the middle finger and the floor when the patient stands upright, heels, buttocks and shoulders against the wall, and bends sideways without lifting the opposite foot off the ground.

Assessment of functional disability related to low back pain

时间窗: 12 weeks

Functional disability of each patient will be measured using Oswestry disability questionnaire. It is a valid and reliable tool consists of 10 multiple choice questions for back pain; subjects selected one sentence out of six that best describe her pain, higher scores indicated great pain. Scores of minimal disability:(0-20%), Scores of moderate disability: (20%- 40%), Scores of severe disability: (40% - 60%), Scores of crippled subjects: (60% - 80%), and Scores of patients confined to bed (80%-100%).

次要结局

  • Assessment of quality of life(12 weeks)
  • Measurement of lumbar Bone Mineral Density (BMD)(12 weeks)

研究者

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

Hanan Karamallah Mohamed Abdelkawy

principal investigator

Cairo University

研究点 (1)

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