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CompletedNCT01182571Updated Aug 30, 2010

Exploration of Fatigue, Uncertainty, Depression and Quality of Life in Heart Transplantation Recipients

An observational study in Heart Transplantation, sponsored by National Taiwan University Hospital. Completed at 1 site in Taiwan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-08-30.

Sponsored by National Taiwan University Hospital · Observational

Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
127
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to explore the fatigue, uncertainty, depression and quality of life in heart transplant recipients, and associated factors of quality of life .

Read the detailed description

The purpose of this study is to explore the symptom distress, fatigue, depression, uncertainty, and quality of life in heart transplant recipients, and associated factors of quality of life (QOL). The eligible patients are (1)who undergone heart transplantation were recruited from the Department of Cardiac Surgery, Nation Taiwan University Hospital,(2)18 year old or older. A set of questionnaire with the Transplant Symptom Frequency and Symptom Distress Scale, Hospital Anxiety and Depression Scale (HADS) , Fatigue Symptom Inventory (FSI), Mishel's Uncertainty Scale, and 12-item Short-Form Health Survey (SF-12) were used to collected symptom distress, fatigue, depression, uncertainty, and QOL .

02

Conditions studied

  • Heart Transplantation

Keywords

  • Heart Transplantation
  • Symptom Distress
  • Fatigue
  • Depression
  • Quality Of Life.
03

In context

Fatigue

1,860 studies on the registry are indexed under Fatigue; 376 are open to participants now.

This study's enrollment of 127 is above the median of 100 across 367 observational studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The outpatients who undergone heart transplantation were recruited from the Department of Cardiac Surgery

Inclusion criteria

  • Clinical diagnosis of heart transplantation
  • Adults 18 years of age

Exclusion criteria

Exclusion Criteria:

  • The woman who are pregnant
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
127 participants (actual)

Groups and cohorts

  • heart transplantation
06

What researchers measure

Primary outcomes

  1. The SF12 Health survey

    It was used to measure quality of life

    Time frame: 1 month

  2. Transplant Symptom Frequency and Symptom Distress Scale

    it was used to measure symptom distress.

    Time frame: 1 week

  3. Fatigue Symptom Inventory

    It was used to measure level of fatigue.

    Time frame: 1 week

  4. Hospital Anxiety and Depression Scale (HADS)

    It was used to measure level of anxiety and depression.

    Time frame: 1month

  5. Illness Uncertainty Scale

    It was used to measure level of uncertainty.

    Time frame: 1 month

07

Study locations

1 site
  • National Taiwan University Hospital
    Taipei, 10051, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 30, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01182571
Lead sponsor
National Taiwan University Hospital
First posted
Aug 17, 2010
Start date
Oct 2008
Primary completion
Aug 2009
Completion
Aug 2009
Last update
Aug 30, 2010

Study contacts

Shiow-Ching Shun, PhD
principal investigator · National Taiwan University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2010. You cannot join it, but the record below documents what was studied.

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