Rehabilitation Interventions After Cardiac Surgery in Older Adults
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
This randomized controlled trial aims to investigate the effects of foot massage and kinesio taping on functional performance and kinesiophobia in older adults following cardiac surgery. Early mobilization after cardiac surgery is essential for improving recovery outcomes; however, pain, fear of movement (kinesiophobia), and reduced functional capacity may delay rehabilitation in older patients. Participants aged 65 years and older who have undergone cardiac surgery will be randomly assigned to either a foot massage group or a kinesio taping group. The foot massage group will receive daily bilateral foot massage for seven consecutive days, while the kinesio taping group will receive standardized kinesio taping applications to the foot and ankle region during the same period. Functional performance, kinesiophobia, pain intensity, cognitive status, and delirium will be assessed using validated outcome measures, including the Timed Up and Go test, Tampa Scale for Kinesiophobia, Visual Analog Scale, Standardized Mini-Mental Test, and Nursing Delirium Screening Scale. Assessments will be conducted preoperatively and on the seventh postoperative day. The study aims to determine whether non-pharmacological, easily applicable interventions such as foot massage and kinesio taping can enhance functional recovery, reduce fear of movement, and support early mobilization in older adults after cardiac surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
April 16, 2026
CompletedFirst Posted
Study publicly available on registry
April 23, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
April 24, 2026
April 1, 2026
7 months
April 16, 2026
April 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Timed Up and Go (TUG) Test
Functional mobility will be assessed using the Timed Up and Go (TUG) test. The time (in seconds) required for the participant to stand up from a seated position, walk 3 meters, turn around, walk back, and sit down will be recorded. Lower scores indicate better functional performance.
Preoperative baseline and postoperative day 7
Secondary Outcomes (4)
Kinesiophobia
Preoperative baseline and postoperative day 7
Pain Intensity
Preoperative baseline and postoperative day 7
Cognitive Function
Preoperative baseline and postoperative day 7
Delirium Status
Preoperative baseline and postoperative day 7
Study Arms (2)
Foot Massage Group
EXPERIMENTALParticipants will receive bilateral foot massage using the Swedish massage technique for 20 minutes daily over a 7-day postoperative period.
Kinesio Taping Group
EXPERIMENTALParticipants will receive standardized kinesio taping applied to the foot and ankle region twice during a 7-day postoperative period.
Interventions
A standardized Swedish massage technique will be applied to the plantar surface of both feet. The intervention will include stroking and kneading techniques applied from the metatarsal heads to the heel and toes. Each session will last 20 minutes (10 minutes per foot) and will be performed daily for 7 consecutive days by a trained healthcare professional.
Kinesio tape (5 cm width) will be applied to the foot and ankle region using standardized techniques. One strip will be applied around the ankle, and two strips will be applied to support the medial and lateral longitudinal arches of the foot. The tape will be applied with 25-75% tension and will be administered by a certified physiotherapist. Applications will be performed twice during a 7-day postoperative period and monitored regularly.
Eligibility Criteria
You may qualify if:
- Age ≥65 years
- Undergoing cardiac surgery (e.g., coronary artery bypass grafting or valve surgery)
- Conscious and able to cooperate
- Able to provide informed consent
You may not qualify if:
- Presence of neurological disorders (e.g., stroke, Parkinson's disease)
- Lower extremity amputation or severe deformity
- Impaired skin integrity in the application area
- Contraindications to massage or kinesio taping
- Refusal to participate
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Asuman SALTAN
University of Yalova
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
April 16, 2026
First Posted
April 23, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
February 1, 2027
Last Updated
April 24, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share