Effect of Postoperative Telehealth Counseling on Recovery and Self-Care in Geriatric Day Surgery Patients
The Effect of Postoperative Telehealth Counseling on Postoperative Recovery and Self-care Power in Geriatric Patients Undergoing Day Surgery
1 other identifier
interventional
72
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2025
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 9, 2025
CompletedStudy Start
First participant enrolled
March 15, 2025
CompletedFirst Posted
Study publicly available on registry
March 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 15, 2025
CompletedMarch 25, 2025
March 1, 2025
8 months
March 9, 2025
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 INTERVENTIONPatients will only be called weekly to complete the scales.
telehealth counseling application
EXPERIMENTALto provide active counseling by calling weekly by phone on issues that the patient needs
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.
Eligibility Criteria
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
- TC Erciyes Universitylead
- Kirsehir Ahi Evran Universitesicollaborator
Central Study Contacts
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