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The Effects of Postoperative Physician Phone Calls for Hand and Wrist Fractures

The Effects of Postoperative Physician Phone Calls for Hand and Wrist Fractures: a Single-blinded, Prospective, Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03557073
Enrollment
24
Registered
2018-06-14
Start date
2018-01-01
Completion date
2018-12-31
Last updated
2019-02-28

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

Conditions

Hand Injuries, Hand Injuries and Disorders, Trauma

Keywords

Hand injuries, Hand trauma, Patient reported outcomes

Brief summary

This study seeks to determine if postoperative phone calls by a physician affect outcomes in hand surgery.

Detailed description

This study seeks to determine if postoperative phone calls by a physician affect outcomes in hand surgery. Patients who require operative treatment of hand and wrist fractures are randomly assigned to a group that receives a postoperative phone call or the control group that receives the standard postoperative care. Patient reported and medical outcomes are observed starting at 1 month postoperatively.

Interventions

BEHAVIORALPostoperative phone call

The intervention is a phone call on the day following surgery.

Sponsors

Indiana University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Masking description

Both the provider and the outcomes assessor are blinded to participant's study arm.

Intervention model description

Participants are randomized to receiving a postoperative phone call or not receiving a postoperative phone call by a physician.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with isolated injuries of the hand who present to a specific level 1 trauma center in the Midwestern United States * Patients who have planned surgical treatment by a pre-specified group of surgeons

Exclusion criteria

* Patients who have significant trauma to other organ systems proximal to the wrist * Patients who have open (compound) fractures (i.e., bone is exposed) * Children

Design outcomes

Primary

MeasureTime frameDescription
Brief Michigan Hand Questionnaire Score Difference1 month postoperatively.A patient reported measure of hand function on a scale of 1 to 100. 100 indicates better hand function and 1 indicates worse hand function. The measure is obtained form a survey that has been published in multiple peer reviewed articles. This score can be subtracted from preoperative score to obtain a difference in score of preoperative compared to postoperative.

Other

MeasureTime frameDescription
Patient compliance with treatment recommendations1 month postoperativelyPatient compliance with treatment as documented in their medical record. Patients are either compliant or not compliant (values can be 0 or 1), i.e., their physician states that they followed instructions or they did not.
Patient satisfaction with their overall care1 month postoperatively.Patient satisfaction with their overall care, as determined on a 5 point Likert scale. 1 is strongly satisfied whereas 5 is strongly dissatisfied.
Patient complication1 month postoperativelyPatient either has a complication or does not (values can be 0 or 1), i.e., their physician states that they had a complication.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026