Skip to main content
OpenTrials
Completed

NCT Number: NCT07156448

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Taichung Veterans General Hospital

Taichung, Taichung City, 40705, Taiwan

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

  • 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

Treatment and study plan

Multicomponent Exercise Program

Behavioral

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.

Primary outcomes

  1. Timed Up and Go (TUG)

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

    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.

  2. 6-meter walk test (6MWT)

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

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

  3. Functional Reach Test (FRT)

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

    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.

  4. Handgrip strength (HGS)

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

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

  5. Barthel Index (BI)

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

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

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

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

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

Secondary outcomes

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

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

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

  2. EuroQol Visual Analogue Scale (EQ-VAS)

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

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

  3. Spiritual Index of Well-Being (SIWB)

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

    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.

Sponsors and collaborators

Lead sponsor

Taichung Veterans General Hospital

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Sep 5, 2025
Registry last updated
Sep 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.