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Clinical Trials/ACTRN12615000570583
ACTRN12615000570583
Completed
未知

Effectiveness of a telehealth programme of combined physical and psychological training in patients following Hematopoietic Stem Cell Transplant (HSCT) on quality of life improvement: a randomised trial

St Vincents0 sites139 target enrollmentJune 2, 2015
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ConditionsBlood CancerBlood - Haematological diseasesPhysical Medicine / Rehabilitation - Other physical medicine / rehabilitationMental Health - Anxiety

Overview

Phase
未知
Intervention
Not specified
Conditions
Blood Cancer
Sponsor
St Vincents
Enrollment
139
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 2, 2015
End Date
December 30, 2020
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
St Vincents

Eligibility Criteria

Inclusion Criteria

  • •Had an Allogeneic or Autologous Haematological Stem Cell Transplant
  • •\- Male or Female
  • •\- Age range: 18 to 75
  • •\- Patient is at least 6 months post\-transplant.
  • •\- Willingness to give written informed consent and willingness to participate in, and comply with the study.
  • •\- Possesses and is able to use a computer or a tablet with Internet connection

Exclusion Criteria

  • •Patient has severe Graft Versus Host Disease or other medical issues that require regular clinic visits
  • •\-Patient has physical or mental impediments which renders them unable to carry out the programs or assessment tasks,
  • •\-Patient has cardiac disease including arrhythmia
  • •\-Patient is deemed unfit for this study by the patient’s haematologist.
  • •\- Participants who fall in the severe or extremely severe range on psychological screening measures of anxiety and depression
  • •\- Participants with a history of a psychological illness or other condition which may interfere with their ability or limit their capacity to understand the requirements of the study.

Outcomes

Primary Outcomes

Not specified

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