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Not yet recruiting NCT06855927

The Effect of Guided Imagery on Activity-Specific Balance Confidence, Pain, and Psychological Well-Being

No phase Interventional Guided Imagery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Guided Imagery.
Who it may be relevant to
Registry conditions: Guided Imagery. Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

The Effect of Guided Imagery on Activity-Specific Balance Confidence, Pain, and Psychological Well-Being in Elderly Orthopedic Patients: A Randomized Controlled Trial

Overview

The aim of this clinical trial is to evaluate the effect of guided imagery on activity-specific balance confidence, pain, and psychological well-being in elderly orthopedic patients. In the study, guided imagery will be applied by the researchers and will be applied over 2 days for a total of 3 repetitions. The study will be conducted in the postoperative period of the patients.

Interventions

  • Other Guided Imagery
    Guided imagery is a potential healing technique that aims to help individuals mentally visualize positive physical and psychological states.

Primary outcome measures

  • Guided imagery applied to elderly orthopedic patients increases activity-specific balance confidence. [Time frame: 100 minutes]
  • Guided imagery applied to elderly orthopedic patients reduces pain levels. [Time frame: 100 minutes]
  • Guided imagery applied to elderly orthopedic patients increases psychological well-being. [Time frame: 100 minutes]

Eligibility criteria

Inclusion criteria

  • Patients who are open to communication and collaboration,
  • Those who are over 65 years old,
  • Those who have a mini-mental test score of 24 and above,
  • Those who have the same type of analgesic protocol,
  • Those who have a numerical pain score of at least 4 will be included.

Exclusion criteria

  • Patients who have developed any complications,
  • Patients who have hearing, vision and perception problems,
  • Patients who have been diagnosed with any psychiatric disease,
  • Patients who have developed any complications after surgery will be excluded.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Sequential
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06855927 · Osmaniye Korkut Ata University

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗