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RecruitingNCT06806891Updated Feb 4, 2025

Restless Leg Syndrome: Is There a Response to Buddhist Walking Meditation in Hemodialysis

An interventional study of Buddhist walking meditation in Hemolysis and Restless Legs Syndrome, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to participants aged 35 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-02-04.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Mar 2025, 1 year 8 months ago, but the record still lists the study as recruiting.
  • Started Nov 2024; still recruiting 2 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
35 Years to 65 Years
Sex
All
01

Study summary

the restless leg syndrome is a common complaint in person who undergo hemodialysis. Buddhist walking meditation efficacy was not investigated in those population

Read the detailed description

the total participants will be 40. all patients will be on hemodialyis. they complain restless leg syndrome. the participants will be divided to group I which received Buddhist walking meditation. this program of meditation will be 30 minutes thrice weekly. before and after buddhist meditation walking, there will be 5 minutes stretching exercises working as warm up or cooling down respectively. the other group will serve as control one .. the number of patient in every group will be 20. the total duration of Buddhist walking meditation will be 12 weeks.

02

Conditions studied

  • Hemolysis
  • Restless Legs Syndrome
03

In context

Hemolysis

120 studies on the registry are indexed under Hemolysis; 22 are open to participants now.

This study's planned enrollment of 40 is below the median of 49 across 78 interventional studies indexed under Hemolysis.

Browse Hemolysis studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • hemodialysis patient (40)
  • complain of restless leg syndrome
  • non obese patients

Exclusion criteria

Exclusion Criteria:

  • cardiac patients
  • chest diseases
  • mental diseases
  • hepatic diseases
  • lower limb orthopedic hurting
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    group number 1

    the participants will be on hemodialyis. they complain restless leg syndrome. the participants will receive Buddhist walking meditation. this program of meditation will be 30 minutes thrice weekly. before and after Buddhist walking meditation .. the number of patients in the group will be 20. the total duration of Buddhist walking meditation will be 12 weeks.

    Behavioral: Buddhist walking meditation

  • No intervention
    group number 2

    the participants will be on hemodialyis. they complain restless leg syndrome. the number of patients in the group will be 20. this group will be control group that will not receive training .

Interventions

  • BehavioralBuddhist walking meditation

    the participants will be on hemodialyis. they complain restless leg syndrome. the participants will receive Buddhist walking meditation. this program of meditation will be 30 minutes thrice weekly. before and after Buddhist walking meditation .. The number of patients in the group will be 20. the total duration of Buddhist walking meditation will be 12 weeks.

06

What researchers measure

Primary outcomes

  1. international RLS Study Group Rating

    it will assess the severity of the problem (restless leg syndrome)

    Time frame: it will be measured after 12 weeks

Secondary outcomes

  1. Pittsburg sleep quality index

    it will assess sleep quality

    Time frame: it will be measured after 12 weeks

  2. fatigue severity scale

    it will assess fatigue level

    Time frame: it will be measured after 12 weeks

  3. sit to stand test

    it will assess number of sit to stand in 30 seconds

    Time frame: it will be measured after 12 weeks

  4. physical component of short form 12

    a questionnaire will assess physical abilities of patients

    Time frame: it will be measured after 12 weeks

  5. mental component of short form 12

    a questionnaire will assess mental status of patients

    Time frame: it will be measured after 12 weeks

  6. beck depression inventory

    a questionnaire will assess depression status of patients

    Time frame: It will be measured after 12 weeks

  7. Trait Anxiety Inventory

    it will assess anxiety in patients

    Time frame: it will be measured after 12 weeks

  8. diatolic blood pressure

    it will be assessed manually

    Time frame: it will be measured after 12 weeks

  9. systolic blood pressure

    it will be assessed manually

    Time frame: it will be measured after 12 weeks

  10. cortisol

    it will be measured in serum

    Time frame: It will be measured after 12 weeks

  11. C reactive protein

    it will be measured in serum

    Time frame: It will be measured after 12 weeks

  12. nitric oxide

    it will be measured in serum

    Time frame: It will be measured after 12 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2024 (actual). Primary completion is estimated for Mar 2025, 4 months after the start.

Of 28 interventional studies with no phase under Hemolysis, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 35. This study's planned 4 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 29, 2025
First posted
Feb 4, 2025
StartActual
Nov 6, 2024
Primary completionEst.
Mar 6, 2025
CompletionEst.
Mar 6, 2025
Last update
Feb 4, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06806891
Lead sponsor
Cairo University
Responsible party
Ali Mohamed Ali ismail (lecturer of physical therapy for Cardiovascular, Respiratory disorder and Geriatrics, Faculty of Physical Therapy, Cairo University, Cairo University) — Principal investigator
First posted
Feb 4, 2025
Start date
Nov 6, 2024
Primary completion
Mar 6, 2025 (estimated)
Completion
Mar 6, 2025 (estimated)
Last update
Feb 4, 2025

Study contacts

Ali MA Ismail, lecturer
Contact
ali.mohamed@pt.cu.edu.eg
01005154209
alshymaa abdelazim, lecturer
Contact
shimaashaaban30@yahoo.com
01033771553
Ali MA Ismail, lecturer
principal investigator · Cairo University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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