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Calm in the Storm: Reducing Night Pain and Enhancing Sleep Through a Nurse- Led Benson's Relaxation Intervention in Hemodialysis Patients

Calm in the Storm: Reducing Night Pain and Enhancing Sleep Through a Nurse- Led Benson's Relaxation Intervention in Hemodialysis Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07814469
Enrollment
60
Registered
2026-09-11
Start date
2025-01-01
Completion date
2025-04-30
Last updated
2026-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodialysis, Hemodialysis Patient

Keywords

Benson's Relaxation Technique, Hemodialysis, Pain, Sleep Quality, Nurse-Led Intervention

Brief summary

Patients undergoing maintenance hemodialysis (HD) frequently experience persistent pain and sleep disturbances which negatively influence their quality of life and overall wellbeing. Non-pharmacological nurse-led interventions such as Benson's relaxation technique (BRT) may offer a safe and cost-effective approach to alleviate these symptoms. Aim: Evaluate the effect of a nurse-led Benson's relaxation intervention on night pain intensity and sleep quality among HD patients.

Detailed description

Hemodialysis patients commonly experience a substantial symptom burden including high levels of stress, pain, sleep disturbances, and diminished QoL. Despite advances in medical management, these symptoms often remain inadequately addressed through pharmacological approaches alone. Exploring BRT as a complementary, non-pharmacological nursing intervention may help alleviate these symptoms and improve overall well-being. Incorporating such evidence-based, low cost, and easily applicable intervention into routine nursing care may enhance patient comfort, promote psychological wellbeing and improve overall QoL. Furthermore, the study findings are anticipated to support the integration of holistic, patient centered care approaches in nephrology nursing practice and to strengthen the growing body of evidence supporting relaxation-based interventions in chronic disease management

Interventions

OTHERBenson's Relaxation Intervention

Benson's Relaxation Intervention

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

1 arm: control group - 1 arm: study group

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adult male and female patients * aged 20 to 65 years, * undergoing maintenance HD for at least 6 months

Exclusion criteria

* Patients with cognitive impairment and psychiatric disorders * Patients receiving pharmacological or nonpharmacological interventions for sleep

Design outcomes

Primary

MeasureTime frameDescription
night painbaseline before implementation of the BRT, secondly in the second week following four intervention sessions, and thirdly in the fourth week following eight intervention sessionsNight Pain Severity and quality Assessed Using the Short-Form McGill Pain Questionnaire (SF-MPQ)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026