NCT07425314

Brief Summary

This randomized controlled study aims to evaluate the effects of a telerehabilitation-based exercise program on muscle strength, exercise capacity, fatigue level, and cognitive status in adult liver transplant recipients. Liver transplantation is a major surgical procedure, and patients may experience reduced physical capacity, muscle weakness, and fatigue during recovery. Exercise-based rehabilitation may help improve these outcomes, but access to in-person rehabilitation programs may be limited after discharge. Participants will be randomly assigned to either a control group receiving routine post-transplant care or an intervention group participating in a supervised telerehabilitation exercise program. The intervention consists of a 12-week program conducted twice weekly via video communication with a physiotherapist. Outcomes will be assessed at baseline and after completion of the program. The study seeks to determine whether a structured, remotely supervised exercise program can improve functional recovery and reduce fatigue in liver transplant patients, potentially offering an accessible rehabilitation option after hospital discharge.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 12, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 28, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

February 13, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 20, 2026

Completed
Last Updated

February 25, 2026

Status Verified

February 1, 2026

Enrollment Period

11 months

First QC Date

February 13, 2026

Last Update Submit

February 23, 2026

Conditions

Keywords

PhysiotherapyLiver TransplantationTelerehabilitationFunctional CapacityFatigue

Outcome Measures

Primary Outcomes (2)

  • 6-Minute Walk Test (6MWT) Distance

    Change in functional exercise capacity measured by the distance (meters) walked during the 6-minute walk test.

    Baseline (pre-intervention) and end of the 12-week intervention period

  • Fatigue Severity Scale

    Change in fatigue severity measured using the Fatigue Severity Scale (FSS). Total scores range from 9 to 63, with higher scores indicating greater fatigue severity.

    Baseline (pre-intervention) and end of the 12-week intervention period

Secondary Outcomes (3)

  • Peripheral Oxygen Saturation (SpO₂)

    Baseline and end of 12 weeks

  • Montreal Cognitive Assessment (MoCA) Score

    Baseline and end of 12 weeks

  • Heart Rate

    Baseline and end of 12 weeks

Study Arms (2)

Telerehabilitation Exercise Group

EXPERIMENTAL

Participants assigned to this arm received a structured telerehabilitation-based exercise program in addition to routine post-transplant care. The program was conducted for 12 weeks, twice weekly, via real-time video communication with a physiotherapist. Sessions included warm-up exercises, posture and breathing exercises, isometric strengthening exercises, functional movements such as sit-to-stand, walking training, and cool-down stretching. Exercise intensity was maintained at a moderate level and progressed gradually throughout the program.

Behavioral: Telerehabilitation Exercise Group

Control Group

NO INTERVENTION

Participants assigned to this arm continued their routine daily activities and received standard post-transplant care without participating in a structured or supervised exercise or rehabilitation program during the study period.

Interventions

Participants in this group received a structured telerehabilitation-based exercise program delivered under real-time supervision by a physiotherapist. The intervention lasted 12 weeks and was conducted twice weekly via video communication. Each session lasted approximately 30-45 minutes and included warm-up exercises, posture and breathing exercises, isometric strengthening exercises for upper and lower extremities, functional exercises such as sit-to-stand, and walking training, followed by cool-down and stretching. Exercise intensity was maintained at a moderate level based on perceived exertion, and progression was applied throughout the program by increasing repetitions and duration to ensure adaptation and safety. Participants were initially instructed face-to-face before discharge and then continued the program remotely after discharge.

Telerehabilitation Exercise Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adult liver transplant recipients aged 18 years or older
  • Medically stable and cleared for participation in an exercise program
  • Able to communicate and cooperate with the researcher
  • Literate and able to understand instructions
  • No orthopedic or neurological condition that would limit exercise participation
  • Approximately one month post-discharge following liver transplantation
  • Willing to participate and provide informed consent

You may not qualify if:

  • Presence of medical conditions that contraindicate exercise participation
  • Severe cardiovascular, respiratory, neurological, or musculoskeletal disorders that could interfere with the exercise program
  • Cognitive impairment preventing understanding of instructions or participation in assessments
  • Postoperative complications requiring activity restriction
  • Participation in another structured exercise or rehabilitation program during the study period
  • Refusal or inability to provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Inonu University Turgut Ozal Medical Center

Malatya, 4400, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Muscle WeaknessFatigue

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Officials

  • Ilker Demir, PhD

    Inonu University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants were randomly assigned to one of two parallel groups. The intervention group received a structured telerehabilitation-based exercise program in addition to routine post-transplant care, while the control group continued routine daily activities without a supervised exercise intervention. The study followed a parallel assignment design in which participants remained in their allocated group throughout the 12-week intervention period, and outcomes were assessed at baseline and post-intervention.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 13, 2026

First Posted

February 20, 2026

Study Start

October 12, 2024

Primary Completion

September 15, 2025

Study Completion

November 28, 2025

Last Updated

February 25, 2026

Record last verified: 2026-02

Locations