ClinicalTrials.Veeva

Menu

Therapeutic Touch on Pain, Delirium, Sleep, and Physiological Parameters

S

Sibel Oksuz

Status

Completed

Conditions

Delirium
Sleep Disturbance

Treatments

Other: therapeutic touch

Study type

Interventional

Funder types

Other

Identifiers

NCT07404904
Aksaray Hospital

Details and patient eligibility

About

The study was conducted to determine the effects of therapeutic touch applied to intensive care patients on pain, delirium, sleep and physiological parameters.

Full description

This study aims to evaluate the effects of therapeutic touch on pain, delirium, sleep, and physiological parameters in surgical intensive care patients. Patients will be assessed at 24, 48, and 72 hours. The intervention and control groups will be randomized. The intervention group will receive routine care and therapeutic touch, while the control group will receive only routine care. Parameters will be assessed before and after each measurement.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who volunteer to participate in the study,
  • Patients aged 18 and over who receive post-surgical treatment at the Surgical Intensive Care Unit of Aksaray Education and Research Hospital,
  • Patients who do not have communication problems (hearing, speaking, understanding, etc.),
  • Patients who have received treatment in the surgical intensive care unit for at least 72 hours,
  • Patients with RASS: between -3 and +4 and Glasgow coma scale: 10 and above,
  • Patients who use only non-steroidal drugs as analgesics,
  • Patients whose medical diagnosis is not dementia,
  • Patients who do not have a mental state disorder/psychological disease and do not use sleeping pills.

Exclusion criteria

  • Patients who developed complications in the ICU after surgery,
  • Patients who received treatment in the surgical intensive care unit for less than 72 hours.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Randomized control
Experimental group
Description:
Experimental (therapeutic touch)
Treatment:
Other: therapeutic touch
Control
No Intervention group
Description:
Control (routine care)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems