NCT06892769

Brief Summary

This study was planned as a randomized controlled experimental study to evaluate the effect of postoperative telehealth counseling on patient outcomes in geriatric patients undergoing day surgery. Hypotheses of the Study H11: In geriatric patients undergoing day surgery, the postoperative self-care power of the intervention group receiving postoperative telehealth counseling is higher than the control group not receiving counseling. H12: In geriatric patients undergoing day surgery, the postoperative recovery status of the intervention group receiving postoperative telehealth counseling is higher than that of the control group not receiving counseling. Inclusion Criteria;

  • 65 years of age or older,
  • Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
  • No communication problems (no vision and hearing problems),
  • No mental problems,
  • Being able to communicate by telephone (by the patient or relative),
  • Volunteering to participate in the study,
  • Having at most two chronic diseases (Diabetes and Hypertension). Exclusion Criteria;
  • Surgery in emergency conditions,
  • developed complications during the case

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 9, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

March 15, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 25, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2025

Completed
Last Updated

March 25, 2025

Status Verified

March 1, 2025

Enrollment Period

8 months

First QC Date

March 9, 2025

Last Update Submit

March 22, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Postoperatıve recovery process

    Data collection tools Postoperative Recovery Index (PRAI): The index consists of 5 sub-dimensions and 25 items. The sub-dimensions are psychological symptoms, physical activities, general symptoms, bowel symptoms and craving symptoms. When determining the sub-dimension score, the scores of the related items are summed and their arithmetic averages are taken. For the total score, all items are summed and the arith. Maximum Possible Score: If the scoring system for each item is on a scale (for example, 1 to 5), the maximum score for each sub-dimension would be the sum of the highest possible score for each item within that sub-dimension. The total maximum score is the sum of the maximum scores for all 25 items. If each item can score between 1 and 5, the maximum score per item is 5. Maximum score for 25 items: 5 x 25 = 125 (total score) Minimum Possible Score: The minimum score for each item is 1, so the lowest possible score for each sub-dimension is 25 (1 for each of the 25 ite

    postoperative 1st, 2nd, 3rd, 4th week

Study Arms (2)

Routine care

NO INTERVENTION

Patients will only be called weekly to complete the scales.

telehealth counseling application

EXPERIMENTAL

to provide active counseling by calling weekly by phone on issues that the patient needs

Other: telehealth counseling

Interventions

Patients in the intervention group will be called every week (for 4 weeks) and will be trained in line with the determined guide and scales will be filled.

telehealth counseling application

Eligibility Criteria

Age65 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • years of age or older,
  • Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
  • No communication problems (no vision and hearing problems),
  • No mental problems,
  • Being able to communicate by telephone (by the patient or relative),
  • Volunteering to participate in the study,
  • Having at most two chronic diseases (Diabetes and Hypertension).

You may not qualify if:

  • Surgery under emergency conditions,
  • developed complications during the case

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Serdar Şahin

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

March 9, 2025

First Posted

March 25, 2025

Study Start

March 15, 2025

Primary Completion

November 15, 2025

Study Completion

December 15, 2025

Last Updated

March 25, 2025

Record last verified: 2025-03