NCT07548684

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

65
Monitor

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
9mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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 Progress2%
May 2026Feb 2027

First Submitted

Initial submission to the registry

April 16, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
8 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2027

Last Updated

April 24, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

April 16, 2026

Last Update Submit

April 23, 2026

Conditions

Keywords

Foot MassageKinesio TapingCardiac SurgeryOlder AdultsFunctional PerformanceKinesiophobiaPostoperative RehabilitationEarly Mobilization

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

EXPERIMENTAL

Participants will receive bilateral foot massage using the Swedish massage technique for 20 minutes daily over a 7-day postoperative period.

Other: Foot Massage

Kinesio Taping Group

EXPERIMENTAL

Participants will receive standardized kinesio taping applied to the foot and ankle region twice during a 7-day postoperative period.

Other: Kinesio Taping

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.

Foot Massage Group

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.

Kinesio Taping Group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

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

Kinesiophobia

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Study Officials

  • Asuman SALTAN

    University of Yalova

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to two parallel groups: a foot massage group and a kinesio taping group. The foot massage group will receive daily bilateral foot massage, while the kinesio taping group will receive standardized kinesio taping applications to the foot and ankle region. Both interventions will be applied over a 7-day postoperative period. Outcome measures will be assessed preoperatively and on the seventh postoperative day.
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