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NCT07816354Completed

Mindfulness for Saudi Hemodialysis Patients

The Effect of Mindfulness_Based Intervention on Sleep Quality, Emotional Symptoms, and Emotion Regulation Among Saudi Patients Receiving Hemodialysis

Source: ClinicalTrials.gov · Last updated 11 Sept 2026

Brief summary (registry, in English)

This study aims to evaluate whether an MBI improves sleep quality, emotional symptoms (depression, anxiety, stress), emotion regulation, and trait mindfulness among adults with ESRD on HD. A randomized two-arm pre-post design was conducted with N = 38 patients at Dr. Soliman Fakeeh Hospital (DSFH), Saudi Arabia (n = 19 intervention; n = 19 control). The intervention comprised 30-minute guided sessions, 3 times a week for 5 weeks during HD sessions. The control group received the study intervention after the study. Outcomes were assessed at baseline and post-intervention using the Pittsburgh Sleep Quality Index (PSQI), Depression Anxiety Stress Scale-21 (DASS-21), Emotion Regulation Questionnaire (ERQ), and Mindful Attention Awareness Scale (MAAS).

Status (registry)
Completed
Study type
Interventional
Enrollment
38 (actual)
First submitted
7 Sept 2026
Start date
1 Jan 2025
Primary completion date
1 Aug 2025
Lead sponsor
Jordan University of Science and Technology
NCT number
NCT07816354

What you commit to

  • Study type: Interventional
  • Participants enrolled: 38
  • From 1 Jan 2025 to the primary completion date, 1 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Having acute psychiatric illness or substantial cognitive dysfunction

Other

  • Involving in frequent meditation or yoga practice.

Who the study is looking for

  • Being aged 18 or above
  • having a history of maintenance dialysis for three months
  • having the capacity to self-report

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dr. Sulima Fakeeh Hospital
Coordinator of this site? Confirm its status
JeddahSaudi ArabiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.