Manual therapy for low back pain in postmenopausal women with osteopenia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the effectiveness of manual therapy in alleviating low back pain among osteopenic postmenopausal women. It addresses the significant impact of chronic low back pain on daily activities and quality of life during menopause, a period when women are particularly vulnerable to musculoskeletal disorders. The intervention includes manual therapy techniques such as craniosacral and visceral manipulation, alongside calcium supplementation, to potentially relieve pain and improve function. The study will involve women aged 50 to 60 who meet specific eligibility criteria related to their health and pain conditions.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Ambulatory, sedentary, non-smoking women having natural menopause at least 1 year before participation in the study.
2. Their ages will range from 50 to 60 years old.
3. Their BMI will be \> 30 kg/m2.
4. Pain before costal margin and above inferior gluteal fold.
5. Osteopenia.

Exclusion Criteria:

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

Where it's running

• Cairo University
  Giza, Egypt Recruiting

Study contacts

• Study coordinator: Hanan Karamallah Mohamed Abdelkawy, MSc
• Email: Hanan.Karamallah.Mohamed@gmail.com
• Phone: 01125665868

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• A novel multi angular isometric lumbar exercise for chronic low back pain

  This trial tests MAILE, a new lumbar exercise method, to see if it helps adults with nonspecific chronic low back pain more than standard lumbar stabilization and core exercises.

  Recruiting Hamad Medical Corporation · Doha · NCT07908693

• Pain catastrophizing, fear of movement, and activity in postmenopausal women with chronic low back pain

  This observational study looks at how negative pain thoughts and fear of moving relate to how active postmenopausal women with long‑standing low back pain are.

  Recruiting Istanbul Medipol University Hospital · Istanbul, Istanbul · NCT07856498

• Analgesia boost from adding a sacral submultifidus block to SIJ injection

  This study tests whether adding a sacral submultifidus block to a standard image-guided sacroiliac joint injection provides better pain relief and function for adults with chronic SIJ‑related pain.

  Recruiting Fayoum University Hospital · Al Fayyum · NCT07814729

• Telerehabilitation after spine surgery

  This trial tests different ways of delivering post-operative instructions to people who had spinal decompression surgery to see how it affects recovery and healthcare use.

  Recruiting Kuopio University Hospital · Kuopio · NCT07795697

• How patient education helps people with chronic musculoskeletal pain stick to home exercise for pain relief

  A structured patient education program is tested to see if it helps people with chronic low back pain, knee osteoarthritis, and shoulder problems stick with their home exercise plan to relieve pain.

  Recruiting Imam Abdulrahman Bin Faisal University · Dammam, Eastern Province · NCT07764354

• Core endurance vs segmental stabilization for low back pain in recreational athletes

  This trial tests whether core endurance exercises or segmental stabilization exercises better help recreational athletes with non-specific low back pain.

  Recruiting Uskudar University · Istanbul · NCT07760103

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.