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. 2023 Aug 31;2023(8):CD013074. doi: 10.1002/14651858.CD013074.pub2

NCT01620580.

Study name Symptom management program for hemodialysis patients
Methods Study design
  • RCT

  • Duration of follow‐up: 8 weeks

Participants Study characteristics
  • Country: USA

  • Setting: not reported

  • Inclusion criteria

    • ≥ 18 years

    • HD 3 times/week

    • Received HD for ≥ 6 months

    • Read and write English

    • Have telephone service

  • Exclusion criteria

    • History of dementia

    • AIDS

    • Active cancer

    • Inability to give informed consent

Interventions Intervention group
  • Self‐management strategies with 15‐minute discussion


Control group
  • Dietary information (4 units)


Co‐interventions
  • Not reported

Outcomes Planned outcomes
  • Itching: after 8 weeks

  • Tiredness: after 8 weeks

  • Numbness: after 8 weeks

  • Sleep disturbance (difficulty falling asleep and difficulty staying asleep): after 8 weeks

  • Adherence to treatment diary improved social functioning, physical functioning and emotional status: after 8 weeks

  • Feasibility of implementing self‐management intervention: after 5 weeks

Starting date September 2011
Contact information Francess V Danquah
Phone: not reported
Email: not reported
Notes ClinicalTrials.gov Identifier: NCT01620580. Funding: The University of Texas Health Science Center, Houston. Recruitment status: completed