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Clinical Trials/NCT01197313
NCT01197313CompletedNot Applicable

Depression and Quality of Life in Chronic Heart Failure Patients and the Caregivers

National Taiwan University Hospital2 sites in 1 country51 target enrollmentStarted: December 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
51
Locations
2
Primary Endpoint
Psychologic aspect

Study Overview

Brief Summary

Anxiety and depression are often present in patients with chronic heart failure (CHF). This study aimed to evaluate the influence of anxiety and depression on the physical function, disability, and quality of life (QOL) in CHF. This study examined the effects of 8-week home-based exercise on these parameters, and investigated the correlations between these outcome changes.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
20 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Clinical diagnosis of CHF for more than 6 months (NYHA Classes I-III)
  • Medically stable for at least 3 months

Exclusion Criteria

  • Malignancy
  • Psychiatric disease, primary neuromusculoskeletal or respiratory diseases that affected the assessment of functional or exercise capacity
  • Changes in medication occurred during the study period

Outcomes

Primary Outcomes

Psychologic aspect

Time Frame: 8 weeks

Anxiety and depression was measured by Hospital Anxiety and Depression Scale (HADS).

Functional capacity

Time Frame: 8 weeks

Functional capacity was assessed by six-minute walk test (6MWT).

Disability level

Time Frame: 8 weeks

Groningen Activity Restriction Scale (GARS)

Quality of life

Time Frame: 8 weeks

Minnesota Living with Heart Failure Questionnaire (MHFQ) was used to assess quality of life.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (2)

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