Effect of Postoperative Telehealth Counseling on Recovery and Self-Care in Geriatric Day Surgery Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65-90
SponsorTC Erciyes University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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,

Disqualifiers

Surgery under emergency conditions,

developed complications during the case

Trial design

Design model

Parallel

Treatments tested in this trial

  • telehealth counseling

    Other intervention

    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.

Treatment groups

72 Participants
are divided into 2 treatment groups
Group A: Routine careNo intervention 0 interventions
Group B: telehealth counseling applicationExperimental treatment 1 intervention

Trial outcomes

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

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

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

TC Erciyes University

Lead sponsor

Kirsehir Ahi Evran Universitesi

Collaborator

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