Preoperative expectation optimization to reduce postoperative pain and disability after hip surgery.

Preoperative expectation optimization to reduce postoperative pain and disability after hip surgery. - SFB-Hip-O

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00033212

Enrollment

200

Registered

2024-11-28

Start date

2025-07-15

Completion date

Unknown

Last updated

2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

OPS 5-820 Patients who undergo a hip total replacement (THR) due to hip osteoarthritis (ICD-10: M16) M16

Interventions

Group 1: Doc+Video: The patients receive a premedication visit by a physician characterized by warm and competent communication and information about the postoperative course. Additionally, they watch

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: For the study, patients will be included who are indicated for a hip joint endoprotheses surgery due to hip osteoarthritis. Patients voluntarily participate in the study and must meet the criteria for surgical indication according to the AWMF S3 guideline (DGOU, 2021, EKIT-Hüfte).

Exclusion criteria

Exclusion criteria: Patients who have cancer or malignant tumors, as well as those suffering from other incurable or severe illnesses requiring specific causal medical or drug treatment, will be excluded from the study. Additionally, patients with significant cognitive impairment or dementia, severe psychiatric disorders (e.g., schizophrenia), or those with identified drug abuse, including regular opioid consumption, will be excluded (exceptions include ICD-10 diagnosis F45.41: Chronic pain disorder with somatic and psychological factors, or pain-related depressive or anxiety disorders, mild to moderate, such as ICD-10 diagnoses F32.0, F32.1, or temporary opioid use to bridge the time until the surgery).

Design outcomes

Primary

Measure	Time frame
Pain intensity NRS (0-10) Comparison between timepoints T1 (4 days preoperatively) and T3 (4 days postoperatively, discharge from hospital)	—

Secondary

Measure	Time frame
Functional capacity (HHS; Harris, 1969), postoperative recovery (QoR, 11 Items; Kahl et al., 2021), mood (STADI, 40 Items; Laux et al., 2013), sensitivities (SBI; Klinger et al, 1999), self-efficacy (ASES-D, 9 Items; Müller et al, 2003), treatment expectation (GEEE; Rief et al., 2021; SETS; Younger et al., 2012; PR-OP Behandlungserfolg; Stuhlreyer et al., 2022), perceived warmth and competence of the study physician (SCM, 12 Items; Fiske et al., 2007), pain medication intake (pain diary)	—

Measure

Time frame

Functional capacity (HHS; Harris, 1969), postoperative recovery (QoR, 11 Items; Kahl et al., 2021), mood (STADI, 40 Items; Laux et al., 2013), sensitivities (SBI; Klinger et al, 1999), self-efficacy (ASES-D, 9 Items; Müller et al, 2003), treatment expectation (GEEE; Rief et al., 2021; SETS; Younger et al., 2012; PR-OP Behandlungserfolg; Stuhlreyer et al., 2022), perceived warmth and competence of the study physician (SCM, 12 Items; Fiske et al., 2007), pain medication intake (pain diary)

—

Countries

Germany

Contacts

Public ContactRegine Klinger

Universitätsklinikum Hamburg-Eppendorf

r.klinger@uke.de+49 152 22824387

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026