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Clinical Trials in Turkey / NCT07194252
Starting soon Not applicable

The Effect of Guided Imagery Technique on Anxiety, Pain, and Analgesic Use in Total Joint Arthroplasty Patients

NCT07194252 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-09-22
Last updated
2025-09-26

Condition(s) studied

Total Joint Arthroplasty

Investigational drug(s) / intervention(s)

Guided imagery technique application

Guided imagery technique application: Intervention is a guided imagery technique designed for patients undergoing total joint arthroplasty. It will be administered in a total of 4 sessions: once daily on the day before surgery, twice daily on the day of surgery, and once daily on the 2nd and 3rd days after surgery, accompanied by imagery scenarios developed in accordance with the Compact Disc (CD) and literature developed by the Turkish Psychological Association. The study aims to examine its effects on surgical anxiety levels, postoperative pain intensity, and analgesic consumption. This approach is structured as a non-pharmacological method specific to surgical nursing practice and differs from previous similar studies in that it is applied in both the preoperative and postoperative periods using the same sample in the literature.

Study summary

This randomized controlled study will investigate the effects of guided imagery on preoperative anxiety and postoperative pain and analgesic consumption in patients undergoing total joint arthroplasty. Conducted between September 2025 and June 2026 at a public hospital in Zonguldak, Turkey, the study will include patients scheduled for total joint arthroplasty following ethics committee approval. The intervention group will receive guided imagery twice preoperatively and once daily at 48 and 72 hours postoperatively. Outcomes will be assessed using the Surgical Anxiety Scale, surgery-specific anxiety scale, Numerical Rating Scale (NRS), and analgesic consumption tracking.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients who have undergone unilateral arthroplasty surgery, * Without cognitive impairment, * Who speak and write Turkish, * Without hearing or vision problems, * Without any other acute illness causing pain or anxiety, * Who received the same analgesic agent in the treatment protocol during the postoperative period, * And who volunteered to participate in the study will be included. Exclusion Criteria: * Having a diagnosis of chronic pain syndrome or neuropathic pain, * Having a diagnosis of psychiatric illness/being under treatment * Continuous use of analgesic/sedative medication that may affect the pain threshold, * Hearing impairment or severe cognitive impairment that prevents participation in guided imagery applications.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Zonguldak Atatürk State Hospital Zonguldak Turkey (Türkiye)

More Ankara Yildirim Beyazıt University trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07194252 on ClinicalTrials.gov ↗ ← All trials in Turkey