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CompletedNCT07156448Updated Sep 5, 2025

Effectiveness of Exercise Intervention on Physical Function, Psychological Health, Quality of Life, and Spiritual Well-Being in Hospitalized Older Patients

An interventional study of Multicomponent Exercise Program in Hospitalization, Aged 65 Years or Older and Activities of Daily Living, sponsored by Taichung Veterans General Hospital. Completed at 1 site in Taiwan. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2025-09-05.

Sponsored by Taichung Veterans General Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 4 years 1 month after the study started (first participant enrolled Jul 2021, registered Aug 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
65 Years and older
Sex
All
01

Study summary

This study aimed to evaluate the effects of a structured exercise program on physical function, psychological well-being, quality of life, and spiritual well-being in hospitalized older adults. A total of 100 inpatients aged 65 years or older were assigned to either an intervention group or a control group. The intervention group participated in a multicomponent exercise program during hospitalization, including resistance training, stretching, and walking, while the control group received routine care. Assessments were performed before and after the intervention using physical performance tests, questionnaires, and well-being scales. The goal is to determine whether such a program can improve mobility, daily living independence, mood, and overall well-being in older patients during hospitalization.

Read the detailed description

This single-center, parallel-group randomized controlled trial investigated the effects of a structured exercise program on multiple dimensions of health in hospitalized older adults. Eligible participants were adults aged ≥65 years, admitted from the emergency department to two internal medicine wards in a teaching hospital in central Taiwan, able to communicate, capable of standing and walking (with or without assistive devices), and willing to participate in the program.

Participants in the intervention group received a structured, multicomponent exercise program consisting of resistance training, stretching, and walking. The program began on the second day of hospitalization and continued until discharge, with a frequency of five sessions per week. Each session lasted approximately 30 minutes, including about 20 minutes of resistance and stretching exercises targeting major muscle groups through functional movements (e.g., sit-to-stand, leg flexion-extension) and flexibility exercises for the upper arms, back, and posterior legs, performed in 2 to 3 sets of 8 to 12 repetitions. Each session also incorporated approximately 10 minutes of walking, with intensity adjusted according to individual tolerance. All sessions were supervised by trained nurses or physical therapists to ensure correct performance and safety.

The control group received routine inpatient care without structured exercise.

Primary outcomes included measures of physical function (Timed Up and Go test, 6-meter walk test, Functional Reach Test, Handgrip strength, and Barthel Index) and psychological health (5-item Geriatric Depression Scale). Secondary outcomes included quality of life (EQ-5D-3L, EQ Visual Analogue Scale) and spiritual well-being (Spiritual Index of Well-Being). All assessments were conducted at baseline (admission) and before discharge by trained assessors blinded to group allocation.

The study aimed to determine whether implementing a structured exercise program during hospitalization could improve multidimensional health outcomes, and to provide evidence for integrating holistic, non-pharmacological interventions into geriatric inpatient care.

02

Conditions studied

  • Hospitalization
  • Aged 65 Years or Older
  • Activities of Daily Living
  • Depression
  • Quality of Life
  • Spirituality

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Keywords

  • Exercise intervention
  • Physical function
  • Mobility
  • Timed Up and Go
  • Barthel Index
  • Functional Reach Test
  • Handgrip strength
  • Geriatric Depression Scale
  • EQ-5D-3L
  • EQ-VAS
  • Spiritual Index of Well-Being
  • Spiritual well-being
  • Internal medicine ward
  • Older patients
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's enrollment of 100 is above the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Taichung Veterans General Hospital is the lead sponsor of 170 studies on the registry; 37 are open to participants now.

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

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age ≥ 65 years
  • Able to communicate
  • Capable of standing and walking (with or without assistive devices)
  • Willing to participate in both the study and the exercise intervention

Exclusion criteria

Exclusion Criteria:

  • Impaired consciousness
  • Acute inflammatory conditions (e.g., gout, acute myocardial infarction, unstable angina, heart failure)
  • Physician-ordered activity restrictions at admission
  • Diagnosed psychiatric disorders or history of epilepsy
  • Severe disability requiring total assistance in daily life
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    Exercise Intervention Group

    Participants received a structured exercise program during hospitalization, including resistance training, stretching, and walking, delivered five times per week for 30 minutes per session.

    Behavioral: Multicomponent Exercise Program

  • No intervention
    Control Group

    Participants received usual hospital care without additional structured exercise intervention.

Interventions

  • BehavioralMulticomponent Exercise Program

    Participants in the intervention group received a structured, multicomponent exercise program consisting of resistance training, stretching, and walking. The program began on the second day of hospitalization and continued until discharge, with a frequency of five sessions per week. Each session lasted approximately 30 minutes, including about 20 minutes of resistance and stretching exercises targeting major muscle groups through functional movements (e.g., sit-to-stand, leg flexion-extension) and flexibility exercises for the upper arms, back, and posterior legs, performed in 2 to 3 sets of 8 to 12 repetitions. Each session also incorporated approximately 10 minutes of walking, with intensity adjusted according to individual tolerance.

06

What researchers measure

Primary outcomes

  1. Timed Up and Go (TUG)

    Assesses mobility and balance by timing the participant as they rise from a chair, walk 3 meters, turn, walk back, and sit down. Time recorded in seconds; shorter times indicate better performance.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  2. 6-meter walk test (6MWT)

    6-meter walk test (6MWT), which measured gait speed, with speeds \<1.0 m/s suggesting reduced independence

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  3. Functional Reach Test (FRT)

    Assesses dynamic balance by measuring the maximum forward reach distance beyond arm's length while standing, in centimeters. A reach \<15 cm indicates higher fall risk.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  4. Handgrip strength (HGS)

    Measures maximal grip force using a handheld dynamometer, recorded in kilograms. Cut-offs: \<26 kg (men) and \<18 kg (women) indicate sarcopenia.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  5. Barthel Index (BI)

    Assesses independence in activities of daily living (ADL) on a scale of 0-100; higher scores indicate better function.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  6. 5-item Geriatric Depression Scale (GDS-5)

    Self-report questionnaire assessing depressive symptoms. Scores ≥2 suggest probable depression.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

Secondary outcomes

  1. EuroQol 5-Dimension 3-Level (EQ-5D-3L)

    Assesses five health domains (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) on three severity levels.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  2. EuroQol Visual Analogue Scale (EQ-VAS)

    Self-rated health status from 0 (worst imaginable) to 100 (best imaginable).

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

  3. Spiritual Index of Well-Being (SIWB)

    12-item questionnaire with two subscales (self-efficacy and life scheme), scored on a 5-point Likert scale. Higher scores reflect poorer spiritual well-being.

    Time frame: Baseline (Day 2 of hospitalization) and at discharge (within 24 hours prior to hospital discharge, average length of stay 10 days)

07

Study locations

1 site
  • Taichung Veterans General Hospital
    Taichung, Taichung City 40705, Taiwan
08

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data (IPD) underlying the published results, including baseline characteristics and all primary and secondary outcome measures, will be shared. A data dictionary will be provided to describe variable definitions. Data will be available upon reasonable request after publication.

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07156448
Lead sponsor
Taichung Veterans General Hospital
Responsible party
Sponsor
First posted
Sep 5, 2025
Start date
Jul 9, 2021
Primary completion
Mar 5, 2022
Completion
Mar 5, 2022
Last update
Sep 5, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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